Johnson & Johnson – Associate Director, Regulatory Medical Writing – Oncology – Toronto, ON

Company: Johnson & Johnson

Location: Toronto, ON

Expected salary:

Job date: Thu, 17 Jul 2025 22:06:21 GMT

Job description: At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.comJob Function:
Medical Affairs GroupJob Sub Function:
Medical WritingJob Category:
ProfessionalAll Job Posting Locations:
Toronto, Ontario, CanadaJob Description:About Innovative MedicineOur expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements. Visionaries like you work on teams that save lives by developing the medicines of tomorrow.Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.Learn more at https://www.jnj.com/innovative-medicinePlease note that this role is available across multiple countries and may be posted under different requisition numbers to comply with local requirements. While you are welcome to apply to any or all of the postings, we recommend focusing on the specific country(s) that align with your preferred location(s):United States – Requisition Number: R-010375Canada – Requisition Number: R-011450Netherlands, Germany, Spain, France – Requisition Number: R-011453Remember, whether you apply to one or all of these requisition numbers, your applications will be considered as a single submission.This can be a hybrid (3 days in office and 2 remote) OR Remote role available in all countries listed above. While specific cities are listed in the Locations section for reference, please note that they are examples only and do not limit your application. We invite candidates from any location to apply.Remote work options may be considered on a case-by-case basis and if approved by the Company.We are searching for the best talent for Associate Director, Regulatory Medical Writing – Oncology.Purpose:

  • Able to function as a lead writer on any compound independently.
  • Leads in setting functional tactics/strategy.
  • Leads project-level strategy (eg, submission team, global program team, clinical team).
  • May represent therapeutic area (TA) head at high-level and cross-functional TA meetings and has some independent decision-making authority.
  • Able to write and coordinate complex documents within and across TAs independently.
  • Contributes to and champions internal standards, regulatory, and publishing guidelines.
  • Contributes to and champions the improvement of internal systems, tools, and processes.
  • Able to lead process working groups.
  • Able to oversee the work of external contractors.
  • May have additional major responsibility with supervision:

+ Cross-functional, cross-TA, or cross-J&J initiative/collaboration.
+ Larger organizational responsibility (eg, manage a subset of TA).

  • If a people manager:

+ Manages a team of internal medical writers (direct reports).
+ Accountable for the quality of deliverables and compliance of direct reports.
+ Actively participates in resource management and hiring decisions.You will be responsible for:

  • Able to lead compound/submission/indication/disease area writing teams independently.
  • Directly leads or sets objectives for others on team projects and tasks, eg, able to lead Medical Writing (MW) process working groups or Communities of Practice.
  • Writes or coordinates all types of clinical and regulatory documents, taking a proactive or lead role in terms of content and scientific strategy.
  • Establishes and drives document timelines and strategies independently.
  • Guides or trains cross-functional team members on processes and best practices; coaches or mentors more junior writers.
  • Proactively identifies and champions departmental process improvements.
  • May develop and present best practices or innovations to internal or external audiences.
  • May lead cross-functional, cross-TA, or cross-J&J process improvement initiatives.
  • Leads discussions in MW and cross-functional meetings as appropriate (eg, submission team meetings, Global Program Team meetings, study team meetings, clinical team meetings).
  • Maintains and disseminates knowledge of industry, company, and regulatory guidelines.
  • Completes all time reporting, training, metrics database, and project tracking (functional planning) updates as required in relevant company systems.
  • Coaches or mentors more junior staff on document planning, processes, content, and provide peer review as needed.
  • If applicable, has lead MW responsibilities for providing guidance on deliverables, content, etc.
  • Interacts with senior cross-functional colleagues and external partners to strengthen coordination between departments.
  • May represent MW in industry standards working groups.
  • As a MW lead, is the primary point of contact for MW activities for the cross-functional team (eg, clinical).
  • If a people manager:

+ Supervises/manages and is accountable for direct reports.
+ Sets objectives and agrees on goals for direct reports. Provides performance oversight, including feedback on performance and development.
+ Regularly meets with direct reports to ensure appropriate development, projects, assignments, and issues are resolved.
+ Ensures direct report’s adherence to established policies, procedural documents, and templates.

  • Participates in hiring staff, onboarding new staff, conducting career and talent development discussions for staff, goal-setting, end-of-year performance reviews, and compensation planning.

Qualifications / Requirements:

  • A university/college degree in a scientific discipline is required. An advanced degree (eg, Masters, PhD, MD) is preferred.
  • At least 10 years of relevant pharmaceutical/scientific experience is required.
  • At least 8 years of relevant clinical/regulatory medical writing experience is required.
  • Experience in project management and process improvement is required.
  • If a people manager: at least 2 years of people management experience is required.
  • Recognizes how to best interpret, summarize, and present statistical and medical information to ensure quality and accuracy of content in complex document types independently.
  • Resolves complex problems independently.
  • Advanced knowledge and application of regulatory guidance documents such as ICH requirements
  • Interacts with senior cross-functional colleagues and external partners, often requiring coordination across multiple functions and groups.
  • Proactively identifies potential risks and develops strategies to mitigate.
  • Identifies and resolves problems related to development and implementation of new service offerings/deliverables.
  • Ability to serve as the liaison between team members and senior leadership within a TA.
  • Excellent oral and written communication skills.
  • Attention to detail.
  • Expert time management for self, direct reports (if applicable), and teams.
  • Ability to build and maintain solid and productive relationships with cross-functional team members.
  • Expert project management skills, expert project/process leadership.
  • Strong leadership skills (influencing, negotiating, assertiveness, taking initiative, conflict management, change management).
  • Ability to delegate responsibility to junior writers.
  • Ability to lead by example, stay focused and positive, and act with integrity.
  • Ability to internalize and teach CREDO behaviors.
  • Ability to act as change agent and adapt to rapidly changing organizational & business challenges.
  • If a people manager: Strong people management skills.

The anticipated base pay range for this position is 10600 to 184000 CAD.The anticipated base pay range for this position is :
The anticipated base pay range for this position is 10600 to 184000.Additional Description for Pay Transparency:

Johnson & Johnson – Associate Director, Regulatory Medical Writing – Oncology – Toronto, ON

Company: Johnson & Johnson

Location: Toronto, ON

Expected salary:

Job date: Wed, 18 Jun 2025 22:49:22 GMT

Job description: At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.comJob Function:
Medical Affairs GroupJob Sub Function:
Medical WritingJob Category:
ProfessionalAll Job Posting Locations:
Toronto, Ontario, CanadaJob Description:About Innovative MedicineOur expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements. Visionaries like you work on teams that save lives by developing the medicines of tomorrow.Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.Learn more at https://www.jnj.com/innovative-medicinePlease note that this role is available across multiple countries and may be posted under different requisition numbers to comply with local requirements. While you are welcome to apply to any or all of the postings, we recommend focusing on the specific country(s) that align with your preferred location(s):United States – Requisition Number: R-010375Canada – Requisition Number: R-011450Netherlands, Germany, Spain, France – Requisition Number: R-011453Remember, whether you apply to one or all of these requisition numbers, your applications will be considered as a single submission.This can be a hybrid (3 days in office and 2 remote) OR Remote role available in all countries listed above. While specific cities are listed in the Locations section for reference, please note that they are examples only and do not limit your application. We invite candidates from any location to apply.Remote work options may be considered on a case-by-case basis and if approved by the Company.We are searching for the best talent for Associate Director, Regulatory Medical Writing – Oncology.Purpose:

  • Able to function as a lead writer on any compound independently.
  • Leads in setting functional tactics/strategy.
  • Leads project-level strategy (eg, submission team, global program team, clinical team).
  • May represent therapeutic area (TA) head at high-level and cross-functional TA meetings and has some independent decision-making authority.
  • Able to write and coordinate complex documents within and across TAs independently.
  • Contributes to and champions internal standards, regulatory, and publishing guidelines.
  • Contributes to and champions the improvement of internal systems, tools, and processes.
  • Able to lead process working groups.
  • Able to oversee the work of external contractors.
  • May have additional major responsibility with supervision:

+ Cross-functional, cross-TA, or cross-J&J initiative/collaboration.
+ Larger organizational responsibility (eg, manage a subset of TA).

  • If a people manager:

+ Manages a team of internal medical writers (direct reports).
+ Accountable for the quality of deliverables and compliance of direct reports.
+ Actively participates in resource management and hiring decisions.You will be responsible for:

  • Able to lead compound/submission/indication/disease area writing teams independently.
  • Directly leads or sets objectives for others on team projects and tasks, eg, able to lead Medical Writing (MW) process working groups or Communities of Practice.
  • Writes or coordinates all types of clinical and regulatory documents, taking a proactive or lead role in terms of content and scientific strategy.
  • Establishes and drives document timelines and strategies independently.
  • Guides or trains cross-functional team members on processes and best practices; coaches or mentors more junior writers.
  • Proactively identifies and champions departmental process improvements.
  • May develop and present best practices or innovations to internal or external audiences.
  • May lead cross-functional, cross-TA, or cross-J&J process improvement initiatives.
  • Leads discussions in MW and cross-functional meetings as appropriate (eg, submission team meetings, Global Program Team meetings, study team meetings, clinical team meetings).
  • Maintains and disseminates knowledge of industry, company, and regulatory guidelines.
  • Completes all time reporting, training, metrics database, and project tracking (functional planning) updates as required in relevant company systems.
  • Coaches or mentors more junior staff on document planning, processes, content, and provide peer review as needed.
  • If applicable, has lead MW responsibilities for providing guidance on deliverables, content, etc.
  • Interacts with senior cross-functional colleagues and external partners to strengthen coordination between departments.
  • May represent MW in industry standards working groups.
  • As a MW lead, is the primary point of contact for MW activities for the cross-functional team (eg, clinical).
  • If a people manager:

+ Supervises/manages and is accountable for direct reports.
+ Sets objectives and agrees on goals for direct reports. Provides performance oversight, including feedback on performance and development.
+ Regularly meets with direct reports to ensure appropriate development, projects, assignments, and issues are resolved.
+ Ensures direct report’s adherence to established policies, procedural documents, and templates.

  • Participates in hiring staff, onboarding new staff, conducting career and talent development discussions for staff, goal-setting, end-of-year performance reviews, and compensation planning.

Qualifications / Requirements:

  • A university/college degree in a scientific discipline is required. An advanced degree (eg, Masters, PhD, MD) is preferred.
  • At least 10 years of relevant pharmaceutical/scientific experience is required.
  • At least 8 years of relevant clinical/regulatory medical writing experience is required.
  • Experience in project management and process improvement is required.
  • If a people manager: at least 2 years of people management experience is required.
  • Recognizes how to best interpret, summarize, and present statistical and medical information to ensure quality and accuracy of content in complex document types independently.
  • Resolves complex problems independently.
  • Advanced knowledge and application of regulatory guidance documents such as ICH requirements
  • Interacts with senior cross-functional colleagues and external partners, often requiring coordination across multiple functions and groups.
  • Proactively identifies potential risks and develops strategies to mitigate.
  • Identifies and resolves problems related to development and implementation of new service offerings/deliverables.
  • Ability to serve as the liaison between team members and senior leadership within a TA.
  • Excellent oral and written communication skills.
  • Attention to detail.
  • Expert time management for self, direct reports (if applicable), and teams.
  • Ability to build and maintain solid and productive relationships with cross-functional team members.
  • Expert project management skills, expert project/process leadership.
  • Strong leadership skills (influencing, negotiating, assertiveness, taking initiative, conflict management, change management).
  • Ability to delegate responsibility to junior writers.
  • Ability to lead by example, stay focused and positive, and act with integrity.
  • Ability to internalize and teach CREDO behaviors.
  • Ability to act as change agent and adapt to rapidly changing organizational & business challenges.
  • If a people manager: Strong people management skills.

The anticipated base pay range for this position is 10600 to 184000 CAD.The anticipated base pay range for this position is :
The anticipated base pay range for this position is 10600 to 184000.Additional Description for Pay Transparency:

Digital Content Design Lead (UX Writing) – Royal Bank of Canada – Toronto, ON

Company: Royal Bank of Canada

Location: Toronto, ON

Expected salary:

Job date: Fri, 23 May 2025 06:23:50 GMT

Job description: Job SummaryJob DescriptionWhat is the Opportunity?RBC Insurance is looking for a Content Design Lead to join our digital design team within Strategy, Digital, and Data. In this role, you will make complex, ‘legalese’ content and UX copy intuitive, inclusive, and meaningful in collaboration with our designers, product team, communications, and marketing. We’re looking for someone who is both a strategic thinker and hands-on doer who can take a human-centred approach to the user journey for both clients and advisors. As part of this position, you’ll write both transactional and marketing copy and set the standards and guidelines to enable a consistent and customer-centric voice across our digital experiences. This is a hybrid role where you’ll be both an individual contributor while also being a manager for 1-2 direct reports.What Will You Do?

  • Create strategies and artifacts (e.g. Digital style guide) to highlight content best practices to ensure an engaging and consistent user experience across all channels
  • Craft clear, succinct, and human-centric UX copy that balances our business goals and user needs, elevating RBC Insurance’s brand wherever possible
  • Write short and long-form copy for a variety of digital experiences for clients and advisors including online applications, website content, advisor portals, and emails
  • Collaborate with key stakeholders including different lines of businesses, digital product, as well as legal and compliance to meet various goals and requirements
  • Apply the principles and technical knowledge of Accessibility and Inclusive Design in content creation for web channels
  • Create supporting documents for French translation and/or support optimizing localization
  • Work with design researchers on using qualitative and quantitative insights to inform content and UX copy decisions, including A/B testing
  • Collaborate with product designers to shape other non-textual content such as interaction patterns, iconography, information graphics, and imagery

What Will You Need to Succeed?Must haves

  • An undergraduate degree in Literature/English, Psychology, Design, Linguistics, Journalism, HCI, or a related field and/or equivalent experience
  • 7+ years of experience in UX writing, content design, or a similar role
  • A portfolio that showcases your work, with an emphasis on digital experiences
  • Fluency in English
  • Strong understanding of how to apply copy and content design to the client and/or advisor lifecycle
  • Experience working within a highly regulated industry, with legal teams or subject matter with complex terms and requirements

Nice to haves

  • Experience contributing to the launch of digital experiences within an agile environment
  • Fluency in French

What’s in it for you

  • A Total Rewards program that includes flexible benefits, work/life balance and career development programs and investment and retirement savings plans
  • Competitive pay and high-earning potential
  • All the tools, training, and team support you need to grow your business and career
  • Flexible work/life balance options
  • Sophisticated RBCI software tools to boost your productivity and grow your business

RBC Insurance is an organization that succeeds by bringing out the best in its people. You’ll be part of a supportive, inclusive team that shares common values – including a fundamental respect for each other. At the heart of this is a commitment to diversity. RBC respects and responds to the many competing and evolving priorities in our lives – so you can focus on what you can do best – putting clients first.Job SkillsAdditional Job DetailsAddress: 180 WELLINGTON ST W:TORONTOCity: TORONTOCountry: CanadaWork hours/week: 37.5Employment Type: Full timePlatform: INSURANCEJob Type: RegularPay Type: SalariedPosted Date: 2025-05-21Application Deadline: 2025-06-11Note: Applications will be accepted until 11:59 PM on the day prior to the application deadline date aboveInclusion and Equal Opportunity EmploymentAt RBC, we believe an inclusive workplace that has diverse perspectives is core to our continued growth as one of the largest and most successful banks in the world. Maintaining a workplace where our employees feel supported to perform at their best, effectively collaborate, drive innovation, and grow professionally helps to bring our Purpose to life and create value for our clients and communities. RBC strives to deliver this through policies and programs intended to foster a workplace based on respect, belonging and opportunity for all.Join our Talent CommunityStay in-the-know about great career opportunities at RBC. Sign up and get customized info on our latest jobs, career tips and Recruitment events that matter to you.Expand your limits and create a new future together at RBC. Find out how we use our passion and drive to enhance the well-being of our clients and communities at .

Job Summary: Content Design Lead at RBC Insurance

Overview:
RBC Insurance is seeking a Content Design Lead to enhance user experience by making complex content accessible and meaningful. This hybrid role involves both hands-on content creation and management of 1-2 direct reports.

Key Responsibilities:

  • Develop content strategies and guidelines for a consistent user experience.
  • Create clear, human-centric UX and marketing copy for various digital channels.
  • Collaborate with stakeholders, including legal and compliance teams, to align on content requirements.
  • Implement accessibility and inclusive design principles in content creation.
  • Support translation efforts, especially for French content.
  • Leverage insights from research and A/B testing to inform content decisions.
  • Work alongside product designers to shape visual and interactive content elements.

Qualifications:

  • Must-haves:

    • Degree in a relevant field or equivalent experience.
    • 7+ years in UX writing or content design.
    • Digital portfolio showcasing relevant work.
    • Fluency in English and understanding of content design in regulated industries.

  • Nice-to-haves:

    • Experience in agile digital product launches.
    • Fluency in French.

Benefits:

  • Flexible benefits and work/life balance.
  • Competitive salary and earning potential.
  • Comprehensive support for career growth.
  • Inclusive work environment promoting diversity.

Additional Details:

  • Location: Toronto, Canada.
  • Employment Type: Full-time, 37.5 hours/week.
  • Application Deadline: June 11, 2025.

Commitment to Inclusion:
RBC values diversity and aims to create a supportive workplace where employees thrive and innovate collaboratively.

Johnson & Johnson – Associate Director, Regulatory Medical Writing – Oncology – Toronto, ON

Company: Johnson & Johnson

Location: Toronto, ON

Expected salary:

Job date: Sun, 27 Apr 2025 05:54:45 GMT

Job description: At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.comJob Function: Medical Affairs GroupJob Sub Function: Medical WritingJob Category: ProfessionalAll Job Posting Locations: Toronto, Ontario, CanadaJob Description:About Innovative MedicineOur expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements. Visionaries like you work on teams that save lives by developing the medicines of tomorrow.Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.Learn more at https://www.jnj.com/innovative-medicinePlease note that this role is available across multiple countries and may be posted under different requisition numbers to comply with local requirements. While you are welcome to apply to any or all of the postings, we recommend focusing on the specific country(s) that align with your preferred location(s):United States – Requisition Number: R-010375Canada – Requisition Number: R-011450Netherlands, Germany, Spain, France – Requisition Number: R-011453Remember, whether you apply to one or all of these requisition numbers, your applications will be considered as a single submission.This can be a hybrid (3 days in office and 2 remote) OR Remote role available in all countries listed above. While specific cities are listed in the Locations section for reference, please note that they are examples only and do not limit your application. We invite candidates from any location to apply.Remote work options may be considered on a case-by-case basis and if approved by the Company.We are searching for the best talent for Associate Director, Regulatory Medical Writing – Oncology.Purpose:Able to function as a lead writer on any compound independently.Leads in setting functional tactics/strategy.Leads project-level strategy (eg, submission team, global program team, clinical team).May represent therapeutic area (TA) head at high-level and cross-functional TA meetings and has some independent decision-making authority.Able to write and coordinate complex documents within and across TAs independently.Contributes to and champions internal standards, regulatory, and publishing guidelines.Contributes to and champions the improvement of internal systems, tools, and processes.Able to lead process working groups.Able to oversee the work of external contractors.May have additional major responsibility with supervision:Cross-functional, cross-TA, or cross-J&J initiative/collaboration.Larger organizational responsibility (eg, manage a subset of TA).If a people manager:Manages a team of internal medical writers (direct reports).Accountable for the quality of deliverables and compliance of direct reports.Actively participates in resource management and hiring decisions.You will be responsible for:Able to lead compound/submission/indication/disease area writing teams independently.Directly leads or sets objectives for others on team projects and tasks, eg, able to lead Medical Writing (MW) process working groups or Communities of Practice.Writes or coordinates all types of clinical and regulatory documents, taking a proactive or lead role in terms of content and scientific strategy.Establishes and drives document timelines and strategies independently.Guides or trains cross-functional team members on processes and best practices; coaches or mentors more junior writers.Proactively identifies and champions departmental process improvements.May develop and present best practices or innovations to internal or external audiences.May lead cross-functional, cross-TA, or cross-J&J process improvement initiatives.Leads discussions in MW and cross-functional meetings as appropriate (eg, submission team meetings, Global Program Team meetings, study team meetings, clinical team meetings).Maintains and disseminates knowledge of industry, company, and regulatory guidelines.Completes all time reporting, training, metrics database, and project tracking (functional planning) updates as required in relevant company systems.Coaches or mentors more junior staff on document planning, processes, content, and provide peer review as needed.If applicable, has lead MW responsibilities for providing guidance on deliverables, content, etc.Interacts with senior cross-functional colleagues and external partners to strengthen coordination between departments.May represent MW in industry standards working groups.As a MW lead, is the primary point of contact for MW activities for the cross-functional team (eg, clinical).If a people manager:Supervises/manages and is accountable for direct reports.Sets objectives and agrees on goals for direct reports. Provides performance oversight, including feedback on performance and development.Regularly meets with direct reports to ensure appropriate development, projects, assignments, and issues are resolved.Ensures direct report’s adherence to established policies, procedural documents, and templates.Participates in hiring staff, onboarding new staff, conducting career and talent development discussions for staff, goal-setting, end-of-year performance reviews, and compensation planning.Qualifications / Requirements:A university/college degree in a scientific discipline is required. An advanced degree (eg, Masters, PhD, MD) is preferred.At least 10 years of relevant pharmaceutical/scientific experience is required.At least 8 years of relevant clinical/regulatory medical writing experience is required.Experience in project management and process improvement is required.If a people manager: at least 2 years of people management experience is required.Recognizes how to best interpret, summarize, and present statistical and medical information to ensure quality and accuracy of content in complex document types independently.Resolves complex problems independently.Advanced knowledge and application of regulatory guidance documents such as ICH requirementsInteracts with senior cross-functional colleagues and external partners, often requiring coordination across multiple functions and groups.Proactively identifies potential risks and develops strategies to mitigate.Identifies and resolves problems related to development and implementation of new service offerings/deliverables.Ability to serve as the liaison between team members and senior leadership within a TA.Excellent oral and written communication skills.Attention to detail.Expert time management for self, direct reports (if applicable), and teams.Ability to build and maintain solid and productive relationships with cross-functional team members.Expert project management skills, expert project/process leadership.Strong leadership skills (influencing, negotiating, assertiveness, taking initiative, conflict management, change management).Ability to delegate responsibility to junior writers.Ability to lead by example, stay focused and positive, and act with integrity.Ability to internalize and teach CREDO behaviors.Ability to act as change agent and adapt to rapidly changing organizational & business challenges.If a people manager: Strong people management skills.The anticipated base pay range for this position is 10600 to 184000 CAD.The anticipated base pay range for this position is : The anticipated base pay range for this position is 10600 to 184000.Additional Description for Pay Transparency:

Johnson & Johnson – Analyst II, Regulatory Medical Writing – Toronto, ON

Company: Johnson & Johnson

Location: Toronto, ON

Expected salary:

Job date: Sat, 12 Apr 2025 01:40:31 GMT

Job description: At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.comJob Function: Medical Affairs GroupJob Sub Function: Medical WritingJob Category: ProfessionalAll Job Posting Locations: Toronto, Ontario, CanadaJob Description:Analyst II, Regulatory Medical WritingAbout Innovative MedicineOur expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements. Visionaries like you work on teams that save lives by developing the medicines of tomorrow. Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way. Learn more atPlease note that this role is available across multiple countries and may be posted under different requisition numbers to comply with local requirements. While you are welcome to apply to any or all of the postings, we recommend focusing on the specific country(s) that align with your preferred location(s):

  • United Kingdom – Requisition Number: R- 008760
  • EU (e.g., Belgium, Finland, France, Germany, Netherlands) – Requisition Number: R-009040
  • Switzerland – Requisition Number: R-009039
  • United States – Requisition Number: R-009045
  • Canada – Requisition Number: R-009050

Remember, whether you apply to one or all of these requisition numbers, your applications will be considered as a single submission.This is a hybrid or remote role available in all locations within Europe and North America. While specific cities are listed in the locations section for reference, please note that they are examples only and do not limit your application. We invite candidates from any location to apply. Remote work options may be considered on a case-by-case basis and if approved by the Company.We are searching for the best talent for Analyst II, Regulatory Medical Writing.As Analyst II, Regulatory Medical Writing, you will support one or more of our therapeutic areas (Oncology, Immunology, Neuroscience, Cardiopulmonary, and Specialty Ophthalmology). Within our Regulatory Medical Writing team, you will join a cohort of writers undergoing internal training to author diverse regulatory medical writing documents. The target start date is 1 September 2025.Purpose:

  • Develop within the medical writing role within the pharmaceutical industry.
  • Work in a team environment and matrix.
  • Gain knowledge and apply internal standards, regulatory, and publishing guidelines.
  • Learn and use internal systems, tools, and processes.
  • Write and coordinate basic documents and help to prepare more complex documents.
  • Perform routine tasks per established procedures.

You will be responsible for:

  • Write and coordinate clinical documents such as protocols, clinical study reports, tables of studies, narratives, and investigator’s brochures with oversight.
  • Perform document QC, literature searches, and other tasks.
  • Work in a matrix environment and gain an understanding of the medical writing responsibilities on project teams.
  • Partner with experienced colleagues on document planning, timelines, and content development according to internal processes.
  • Participate in or lead cross-functional document planning and review meetings independently or with oversight.
  • May participate in initiatives to improve medical writing processes and standards.
  • Acquire, maintain, and apply knowledge of industry, company, and regulatory guidelines.
  • Regularly meet with manager and mentors and attend departmental meetings.

Qualifications/Requirements:

  • A university/college degree in a scientific discipline is the minimum requirement, with an advanced degree (eg, Master’s degree, PhD, MD) preferred.
  • At least 2 years of relevant pharmaceutical/scientific experience is required.
  • Strong oral and written communication skills in English.
  • Ability to understand, interpret, and summarize scientific or medical data.
  • Ability to function in a team environment and to build solid and positive relationships with cross‐functional team members.
  • Demonstrated problem-solving skills.
  • Strong attention to detail.
  • Strong time management and project/process management skills.
  • Demonstrated learning agility.
  • Sound knowledge of Microsoft Office programs (eg, Microsoft Word, Excel, PowerPoint, Outlook)

Benefits:We offer a competitive salary and extensive benefits package. The health and well-being of our employees is a priority, we have a flexible working environment as we value work-life balance. We offer career development opportunities for those who want to grow and be part of our organisation. For additional general information on company benefits, please go to: https://www.careers.jnj.com/employee-benefitsAll qualified applicants will be considered for employment without regard to any other characteristic protected by law. We will ensure that individuals with disabilities are provided a reasonable accommodation to participate in the job application or interview process, to perform important job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodations.#LI-Hybrid#LI-Remote

Johnson & Johnson – Analyst, Regulatory Medical Writing – Toronto, ON

Company: Johnson & Johnson

Location: Toronto, ON

Expected salary:

Job date: Sat, 12 Apr 2025 04:08:09 GMT

Job description: At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.comJob Function: Medical Affairs GroupJob Sub Function: Medical WritingJob Category: ProfessionalAll Job Posting Locations: Toronto, Ontario, CanadaJob Description:Analyst, Regulatory Medical WritingAbout Innovative MedicineOur expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements. Visionaries like you work on teams that save lives by developing the medicines of tomorrow. Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way. Learn more atPlease note that this role is available across multiple countries and may be posted under different requisition numbers to comply with local requirements. While you are welcome to apply to any or all of the postings, we recommend focusing on the specific country(s) that align with your preferred location(s):

  • United Kingdom – Requisition Number: R-008756
  • EU (e.g., Belgium, Finland, France, Germany, Netherlands) – Requisition Number: R-009077
  • Switzerland – Requisition Number: R-009084
  • United States – Requisition Number: R-009090
  • Canada – Requisition Number: R-009088

Remember, whether you apply to one or all of these requisition numbers, your applications will be considered as a single submission.This is a hybrid or remote role available in all locations within Europe and North America. While specific cities are listed in the locations section for reference, please note that they are examples only and do not limit your application. We invite candidates from any location to apply. Remote work options may be considered on a case-by-case basis and if approved by the Company.We are searching for the best talent for Analyst, Regulatory Medical Writing.As Analyst, Regulatory Medical Writing, you will support one or more of our therapeutic areas (Oncology, Immunology, Neuroscience, Cardiopulmonary, and Specialty Ophthalmology). Within our Regulatory Medical Writing team, you will join a cohort of writers undergoing internal training to author diverse regulatory medical writing documents. The target start date is 1 September 2025.Purpose:

  • Learn the regulatory medical writing role and pharmaceutical industry and business.
  • Learn to work in a team environment and matrix.
  • Learn internal standards, regulatory, and publishing guidelines.
  • Learn internal systems, tools, and processes.
  • Help to prepare sections of documents and prepare basic documents under supervision.
  • Assist with routine tasks per established procedures.

You will be responsible for:

  • Prepare components of clinical and regulatory documents and write basic documents such as tables of studies, narratives, protocol amendments, investigator’s brochure updates and addenda under supervision.
  • May assist with document QC, abbreviations, references, literature searches, and other tasks.
  • Learn how to interpret, summarize, and present statistical and medical information.
  • Learn to work in a matrix environment and gain an understanding of the medical writing responsibilities on project teams.
  • Attend cross-functional meetings with other writers as appropriate (eg, project kick-off and review meetings).
  • Learn and adhere to SOPs, templates, best practices, policies, and Medical Writing Style Guide.
  • Regularly meet with manager and mentors and attend departmental meetings.

Qualifications / Requirements:

  • A university/college degree in a scientific discipline is the minimum requirement, with an advanced degree (eg, Master’s degree, PhD, MD) preferred.
  • Strong oral and written communication skills in English.
  • Ability to understand and summarize scientific data.
  • Ability to function in a team environment and to build solid and positive relationships with co-workers.
  • Demonstrated problem-solving skills.
  • Attention to detail.
  • Organizational skills and time management skills.
  • Demonstrated learning agility.
  • Ability to learn and apply knowledge of regulatory guidance documents such as ICH requirements.
  • Working knowledge of Microsoft Office programs (eg, Microsoft Word, Excel, PowerPoint, Outlook).

BenefitsWe offer a competitive salary and extensive benefits package. The health and well-being of our employees is a priority, we have a flexible working environment as we value work-life balance. We offer career development opportunities for those who want to grow and be part of our organisation. For additional general information on company benefits, please go to: https://www.careers.jnj.com/employee-benefitsAll qualified applicants will be considered for employment without regard to any other characteristic protected by law. We will ensure that individuals with disabilities are provided a reasonable accommodation to participate in the job application or interview process, to perform important job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodations.#LI-Hybrid#LI-Remote

Johnson & Johnson – Analyst II, Regulatory Medical Writing – Toronto, ON

Company: Johnson & Johnson

Location: Toronto, ON

Expected salary:

Job date: Sat, 12 Apr 2025 22:23:31 GMT

Job description: At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.comJob Function:
Medical Affairs GroupJob Sub Function:
Medical WritingJob Category:
ProfessionalAll Job Posting Locations:
Toronto, Ontario, CanadaJob Description:Analyst II, Regulatory Medical WritingAbout Innovative MedicineOur expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements. Visionaries like you work on teams that save lives by developing the medicines of tomorrow. Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way. Learn more at https://www.jnj.com/innovative-medicinePlease note that this role is available across multiple countries and may be posted under different requisition numbers to comply with local requirements. While you are welcome to apply to any or all of the postings, we recommend focusing on the specific country(s) that align with your preferred location(s):

  • United Kingdom – Requisition Number: R- 008760
  • EU (e.g., Belgium, Finland, France, Germany, Netherlands) – Requisition Number: R-009040
  • Switzerland – Requisition Number: R-009039
  • United States – Requisition Number: R-009045
  • Canada – Requisition Number: R-009050

Remember, whether you apply to one or all of these requisition numbers, your applications will be considered as a single submission.This is a hybrid or remote role available in all locations within Europe and North America. While specific cities are listed in the locations section for reference, please note that they are examples only and do not limit your application. We invite candidates from any location to apply. Remote work options may be considered on a case-by-case basis and if approved by the Company.We are searching for the best talent for Analyst II, Regulatory Medical Writing.As Analyst II, Regulatory Medical Writing, you will support one or more of our therapeutic areas (Oncology, Immunology, Neuroscience, Cardiopulmonary, and Specialty Ophthalmology). Within our Regulatory Medical Writing team, you will join a cohort of writers undergoing internal training to author diverse regulatory medical writing documents. The target start date is 1 September 2025.Purpose:

  • Develop within the medical writing role within the pharmaceutical industry.
  • Work in a team environment and matrix.
  • Gain knowledge and apply internal standards, regulatory, and publishing guidelines.
  • Learn and use internal systems, tools, and processes.
  • Write and coordinate basic documents and help to prepare more complex documents.
  • Perform routine tasks per established procedures.

You will be responsible for:

  • Write and coordinate clinical documents such as protocols, clinical study reports, tables of studies, narratives, and investigator’s brochures with oversight.
  • Perform document QC, literature searches, and other tasks.
  • Work in a matrix environment and gain an understanding of the medical writing responsibilities on project teams.
  • Partner with experienced colleagues on document planning, timelines, and content development according to internal processes.
  • Participate in or lead cross-functional document planning and review meetings independently or with oversight.
  • May participate in initiatives to improve medical writing processes and standards.
  • Acquire, maintain, and apply knowledge of industry, company, and regulatory guidelines.
  • Regularly meet with manager and mentors and attend departmental meetings.

Qualifications/Requirements:

  • A university/college degree in a scientific discipline is the minimum requirement, with an advanced degree (eg, Master’s degree, PhD, MD) preferred.
  • At least 2 years of relevant pharmaceutical/scientific experience is required.
  • Strong oral and written communication skills in English.
  • Ability to understand, interpret, and summarize scientific or medical data.
  • Ability to function in a team environment and to build solid and positive relationships with cross‐functional team members.
  • Demonstrated problem-solving skills.
  • Strong attention to detail.
  • Strong time management and project/process management skills.
  • Demonstrated learning agility.
  • Sound knowledge of Microsoft Office programs (eg, Microsoft Word, Excel, PowerPoint, Outlook)

Benefits:We offer a competitive salary and extensive benefits package. The health and well-being of our employees is a priority, we have a flexible working environment as we value work-life balance. We offer career development opportunities for those who want to grow and be part of our organisation. For additional general information on company benefits, please go to: https://www.careers.jnj.com/employee-benefitsAll qualified applicants will be considered for employment without regard to any other characteristic protected by law. We will ensure that individuals with disabilities are provided a reasonable accommodation to participate in the job application or interview process, to perform important job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodations.#LI-Hybrid#LI-Remote

Johnson & Johnson – Analyst, Regulatory Medical Writing – Toronto, ON

Company: Johnson & Johnson

Location: Toronto, ON

Expected salary:

Job date: Sat, 12 Apr 2025 22:59:40 GMT

Job description: At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.comJob Function:
Medical Affairs GroupJob Sub Function:
Medical WritingJob Category:
ProfessionalAll Job Posting Locations:
Toronto, Ontario, CanadaJob Description:Analyst, Regulatory Medical WritingAbout Innovative MedicineOur expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements. Visionaries like you work on teams that save lives by developing the medicines of tomorrow. Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way. Learn more at https://www.jnj.com/innovative-medicinePlease note that this role is available across multiple countries and may be posted under different requisition numbers to comply with local requirements. While you are welcome to apply to any or all of the postings, we recommend focusing on the specific country(s) that align with your preferred location(s):

  • United Kingdom – Requisition Number: R-008756
  • EU (e.g., Belgium, Finland, France, Germany, Netherlands) – Requisition Number: R-009077
  • Switzerland – Requisition Number: R-009084
  • United States – Requisition Number: R-009090
  • Canada – Requisition Number: R-009088

Remember, whether you apply to one or all of these requisition numbers, your applications will be considered as a single submission.This is a hybrid or remote role available in all locations within Europe and North America. While specific cities are listed in the locations section for reference, please note that they are examples only and do not limit your application. We invite candidates from any location to apply. Remote work options may be considered on a case-by-case basis and if approved by the Company.We are searching for the best talent for Analyst, Regulatory Medical Writing.As Analyst, Regulatory Medical Writing, you will support one or more of our therapeutic areas (Oncology, Immunology, Neuroscience, Cardiopulmonary, and Specialty Ophthalmology). Within our Regulatory Medical Writing team, you will join a cohort of writers undergoing internal training to author diverse regulatory medical writing documents. The target start date is 1 September 2025.Purpose:

  • Learn the regulatory medical writing role and pharmaceutical industry and business.
  • Learn to work in a team environment and matrix.
  • Learn internal standards, regulatory, and publishing guidelines.
  • Learn internal systems, tools, and processes.
  • Help to prepare sections of documents and prepare basic documents under supervision.
  • Assist with routine tasks per established procedures.

You will be responsible for:

  • Prepare components of clinical and regulatory documents and write basic documents such as tables of studies, narratives, protocol amendments, investigator’s brochure updates and addenda under supervision.
  • May assist with document QC, abbreviations, references, literature searches, and other tasks.
  • Learn how to interpret, summarize, and present statistical and medical information.
  • Learn to work in a matrix environment and gain an understanding of the medical writing responsibilities on project teams.
  • Attend cross-functional meetings with other writers as appropriate (eg, project kick-off and review meetings).
  • Learn and adhere to SOPs, templates, best practices, policies, and Medical Writing Style Guide.
  • Regularly meet with manager and mentors and attend departmental meetings.

Qualifications / Requirements:

  • A university/college degree in a scientific discipline is the minimum requirement, with an advanced degree (eg, Master’s degree, PhD, MD) preferred.
  • Strong oral and written communication skills in English.
  • Ability to understand and summarize scientific data.
  • Ability to function in a team environment and to build solid and positive relationships with co-workers.
  • Demonstrated problem-solving skills.
  • Attention to detail.
  • Organizational skills and time management skills.
  • Demonstrated learning agility.
  • Ability to learn and apply knowledge of regulatory guidance documents such as ICH requirements.
  • Working knowledge of Microsoft Office programs (eg, Microsoft Word, Excel, PowerPoint, Outlook).

BenefitsWe offer a competitive salary and extensive benefits package. The health and well-being of our employees is a priority, we have a flexible working environment as we value work-life balance. We offer career development opportunities for those who want to grow and be part of our organisation. For additional general information on company benefits, please go to: https://www.careers.jnj.com/employee-benefitsAll qualified applicants will be considered for employment without regard to any other characteristic protected by law. We will ensure that individuals with disabilities are provided a reasonable accommodation to participate in the job application or interview process, to perform important job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodations.#LI-Hybrid#LI-Remote

Johnson & Johnson – Senior Analyst, Regulatory Medical Writing – Immunology – Toronto, ON

Company: Johnson & Johnson

Location: Toronto, ON

Expected salary: $91000 – 147200 per year

Job date: Sat, 08 Mar 2025 08:44:58 GMT

Job description: At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.comJob Function: Medical Affairs GroupJob Sub Function: Medical WritingJob Category: ProfessionalAll Job Posting Locations: Toronto, Ontario, CanadaJob Description:Job DescriptionAbout Innovative MedicineOur expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements. Visionaries like you work on teams that save lives by developing the medicines of tomorrow.Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.Learn more atPlease note that this role is available across multiple countries and may be posted under different requisition numbers to comply with local requirements. While you are welcome to apply to any or all of the postings, we recommend focusing on the specific country(s) that align with your preferred location(s):US – Requisition Number: 2506235426WEurope/India – Requisition Number: R-002023Remember, whether you apply to one or all of these requisition numbers, your applications will be considered as a single submission.Remote work options may be considered on a case-by-case basis and if approved by the Company.We are searching for the best talent for Senior Analyst, Regulatory Medical Writing – Immunology to be in US, Canada, Europe, or India.Purpose:Able to write and coordinate basic and complex documents, independently when working within own therapeutic area (TA), and under supervision when working across TAs.Leads in a team environment and matrix.Able to function as a lead MW on most compounds, under supervision.Actively participates in or leads process working groups.Provides input into functional tactics/strategy (eg, writing teams, process working groups).Highly proficient in the use of internal systems, tools, and processes.You will be responsible for:Writes or coordinates clinical and regulatory documents such as, but not limited to, CSRs, IBs, protocols, summary documents, RMPs, regulatory responses, and briefing documents.Leads cross-functional document planning and review meetings. Interacts with cross-functional colleagues on document content and champions medical writing processes and best practices. Responsible for establishing document timelines and strategies in accordance with internal processes, with some mentorship from functional management and clinical team, as needed.Actively participates in or leads process working groups.Coaches or mentors more junior staff on document planning, processes, and content. Provides peer review as needed.Qualifications / Requirements:A university/college degree in a scientific field is required. An advanced degree (eg, Masters, PhD, MD) is preferred.At least 6 years of relevant pharmaceutical/scientific experience including at least 4 years of regulatory medical writing experience is required.Recognizes how to best interpret, summarize, and present statistical and medical information to ensure quality and accuracy of content in all document types under general supervision.Proficiency in written and spoken English is essential, together with excellent oral and written communication skills.Strong attention to detail.Ability to collaborate with cross-functional global teams across time zones, requiring some flexibility in your daily routine.Builds productive relationships with cross-functional team members.Has strong leadership skills, both in project and process management as well as in time management (influencing, negotiating, assertiveness, taking initiative). Resolves complex problems under supervision.Organizes time well and demonstrates learning agility.The anticipated base pay range for this position is $91,000 to $147,200 CAD.The anticipated base pay range for this position is :Additional Description for Pay Transparency:

Johnson & Johnson – Senior Analyst, Regulatory Medical Writing – Immunology – Toronto, ON

Company: Johnson & Johnson

Location: Toronto, ON

Expected salary: $91000 – 147200 per year

Job date: Sat, 08 Mar 2025 23:01:40 GMT

Job description: At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.comJob Function:
Medical Affairs GroupJob Sub Function:
Medical WritingJob Category:
ProfessionalAll Job Posting Locations:
Toronto, Ontario, CanadaJob Description:Job DescriptionAbout Innovative MedicineOur expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements. Visionaries like you work on teams that save lives by developing the medicines of tomorrow.Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.Learn more at https://www.jnj.com/innovative-medicinePlease note that this role is available across multiple countries and may be posted under different requisition numbers to comply with local requirements. While you are welcome to apply to any or all of the postings, we recommend focusing on the specific country(s) that align with your preferred location(s):US – Requisition Number: 2506235426WEurope/India – Requisition Number: R-002023Remember, whether you apply to one or all of these requisition numbers, your applications will be considered as a single submission.Remote work options may be considered on a case-by-case basis and if approved by the Company.We are searching for the best talent for Senior Analyst, Regulatory Medical Writing – Immunology to be in US, Canada, Europe, or India.Purpose:

  • Able to write and coordinate basic and complex documents, independently when working within own therapeutic area (TA), and under supervision when working across TAs.
  • Leads in a team environment and matrix.
  • Able to function as a lead MW on most compounds, under supervision.
  • Actively participates in or leads process working groups.
  • Provides input into functional tactics/strategy (eg, writing teams, process working groups).
  • Highly proficient in the use of internal systems, tools, and processes.

You will be responsible for:

  • Writes or coordinates clinical and regulatory documents such as, but not limited to, CSRs, IBs, protocols, summary documents, RMPs, regulatory responses, and briefing documents.
  • Leads cross-functional document planning and review meetings. Interacts with cross-functional colleagues on document content and champions medical writing processes and best practices. Responsible for establishing document timelines and strategies in accordance with internal processes, with some mentorship from functional management and clinical team, as needed.
  • Actively participates in or leads process working groups.
  • Coaches or mentors more junior staff on document planning, processes, and content. Provides peer review as needed.

Qualifications / Requirements:

  • A university/college degree in a scientific field is required. An advanced degree (eg, Masters, PhD, MD) is preferred.
  • At least 6 years of relevant pharmaceutical/scientific experience including at least 4 years of regulatory medical writing experience is required.
  • Recognizes how to best interpret, summarize, and present statistical and medical information to ensure quality and accuracy of content in all document types under general supervision.
  • Proficiency in written and spoken English is essential, together with excellent oral and written communication skills.
  • Strong attention to detail.
  • Ability to collaborate with cross-functional global teams across time zones, requiring some flexibility in your daily routine.
  • Builds productive relationships with cross-functional team members.
  • Has strong leadership skills, both in project and process management as well as in time management (influencing, negotiating, assertiveness, taking initiative). Resolves complex problems under supervision.
  • Organizes time well and demonstrates learning agility.

The anticipated base pay range for this position is $91,000 to $147,200 CAD.The anticipated base pay range for this position is :Additional Description for Pay Transparency: