Actalent – Study Director – Kitchener, ON

Company: Actalent

Location: Kitchener, ON

Expected salary: $80000 – 90000 per year

Job date: Wed, 12 Feb 2025 03:26:10 GMT

Job description: Job Title: Study DirectorJob DescriptionAs a Study Director, you will be responsible for managing multiple in vitro assays within the Toxicology department. You will serve as the subject matter expert with respect to assay performance and life cycle management. You will work closely with the operations team to standardize assay workflows, analyze assay trends, and continuously improve assays. Additionally, you will analyze and interpret assay data and prepare client protocols and reports.Responsibilities

  • Oversee assay performance and address assay deviations from set performance indicators.
  • Manage the life cycle of assays.
  • Evaluate, validate, and troubleshoot methods.
  • Maintain and update relevant Standard Operating Procedures (SOPs).
  • Ensure assay precision, accuracy, and reproducibility through appropriate Quality Control (QC) procedures.
  • Lead Root Cause Analysis (RCA) for deviations and repeats.
  • Effectively communicate and coach the operations team.
  • Contribute to the implementation of new Toxicology assays as needed.
  • Interact with clients on technical issues.
  • Oversee the day-to-day assay performance and ensure timely correction of any deviations.
  • Implement, validate, and troubleshoot new High-Throughput (HTP) methods.
  • Ensure that the scientific quality of assays is maintained during production.
  • Follow QC procedures including charting and related measures for Statistical Process Control (SPC).
  • Work with the operations team to determine timelines for specific projects, analyses, and method development.
  • Process analytical data and liaise with the internal statistical department.
  • Communicate analytical results to relevant stakeholders.
  • Discuss technical inquiries with clients in accordance with company policy.
  • Lead RCA investigations and ensure timely resolution identification.
  • Perform duties of the Study Director for Good Laboratory Practice (GLP) studies, coordinating inputs from management, scientific/technical staff, and the Quality Assurance program (QS).
  • Oversee study plan design and approval, including amendments, as well as data collection, analysis, and reporting.
  • Prepare Study Plans/Study Protocols in consultation with the sponsor and internal management.

Essential Skills

  • Master’s degree in Toxicology, Cell Biology, Biochemistry, or Pharmacology.
  • Three or more years of experience in a lab testing environment.
  • Experience in nonclinical toxicology.
  • Experience with in vitro assays.
  • Experience with flow cytometry.
  • Working knowledge of Good Laboratory Practices (GLP) regulations and study management.

Additional Skills & Qualifications

  • Ability to work cooperatively in a team environment.
  • Effective communication skills.
  • Strong problem-solving and troubleshooting abilities.
  • Ability to effectively prioritize and multitask.
  • Experience conducting effective meetings.
  • Ability to communicate effectively with staff and interface with both technical and non-technical personnel.
  • Understanding of Quality System Procedures and Test Methods.

Work EnvironmentThis position is based in both the lab and office, requiring onsite presence with no remote work option.Pay and BenefitsThe pay range for this position is $80000.00 – $90000.00/yr.Workplace TypeThis is a fully onsite position in Kitchener,ON.À propos d’Actalent:Actalent est un chef de file mondial des services d’ingénierie et de sciences et des solutions de talents. Nous aidons les entreprises visionnaires à faire progresser leurs initiatives en matière d’ingénierie et de science en leur donnant accès à des experts spécialisés qui favorisent la mise à l’échelle, l’innovation et la mise en marché rapide. Avec un réseau de près de 30 000 consultants et plus de 4 500 clients aux États-Unis, au Canada, en Asie et en Europe, Actalent est au service d’un grand nombre d’entreprises du classement Fortune 500.La diversité, l’équité et l’inclusionChez Actalent, la diversité et l’inclusion constituent le pont vers l’équité et la réussite de notre personnel. La diversité, l’équité et l’inclusion (DE&I) sont ancrées dans notre culture par :

  • L’embauche des talents diversifiés ;
  • Le maintien d’un environnement inclusif par une autoréflexion permanente ;
  • La mise en place d’une culture de soin, d’engagement, et de reconnaissance par des résultats concrets ;
  • L’assurance des opportunités de croissance pour nos gens.

Actalent est un employeur souscrivant au principe de l’égalité des chances et accepte toutes les candidatures sans tenir compte de la race, du sexe, de l’âge, de la couleur, de la religion, des origines nationales, du statut d’ancien combattant, d’un handicap, de l’orientation sexuelle, de l’identité sexuelle, des renseignements génétiques ou de toute autre caractéristique protégée par la loi.Si vous souhaitez faire une demande d’accommodement raisonnable, tel que la modification ou l’ajustement du processus de demande d’emploi ou d’entrevue à cause d’un handicap, veuillez envoyer un courriel à pour connaître d’autres options d’accommodement.About ActalentActalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.Diversity, Equity & InclusionAt Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I are embedded into our culture through:

  • Hiring diverse talent
  • Maintaining an inclusive environment through persistent self-reflection
  • Building a culture of care, engagement, and recognition with clear outcomes
  • Ensuring growth opportunities for our people

The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email for other accommodation options.

Actalent – Study Director – Kitchener, ON

Company: Actalent

Location: Kitchener, ON

Expected salary: $80000 – 90000 per year

Job date: Wed, 12 Feb 2025 05:30:52 GMT

Job description: Job Title: Study DirectorJob DescriptionAs a Study Director, you will be responsible for managing multiple in vitro assays within the Toxicology department. You will serve as the subject matter expert with respect to assay performance and life cycle management. You will work closely with the operations team to standardize assay workflows, analyze assay trends, and continuously improve assays. Additionally, you will analyze and interpret assay data and prepare client protocols and reports.Responsibilities

  • Oversee assay performance and address assay deviations from set performance indicators.
  • Manage the life cycle of assays.
  • Evaluate, validate, and troubleshoot methods.
  • Maintain and update relevant Standard Operating Procedures (SOPs).
  • Ensure assay precision, accuracy, and reproducibility through appropriate Quality Control (QC) procedures.
  • Lead Root Cause Analysis (RCA) for deviations and repeats.
  • Effectively communicate and coach the operations team.
  • Contribute to the implementation of new Toxicology assays as needed.
  • Interact with clients on technical issues.
  • Oversee the day-to-day assay performance and ensure timely correction of any deviations.
  • Implement, validate, and troubleshoot new High-Throughput (HTP) methods.
  • Ensure that the scientific quality of assays is maintained during production.
  • Follow QC procedures including charting and related measures for Statistical Process Control (SPC).
  • Work with the operations team to determine timelines for specific projects, analyses, and method development.
  • Process analytical data and liaise with the internal statistical department.
  • Communicate analytical results to relevant stakeholders.
  • Discuss technical inquiries with clients in accordance with company policy.
  • Lead RCA investigations and ensure timely resolution identification.
  • Perform duties of the Study Director for Good Laboratory Practice (GLP) studies, coordinating inputs from management, scientific/technical staff, and the Quality Assurance program (QS).
  • Oversee study plan design and approval, including amendments, as well as data collection, analysis, and reporting.
  • Prepare Study Plans/Study Protocols in consultation with the sponsor and internal management.

Essential Skills

  • Master’s degree in Toxicology, Cell Biology, Biochemistry, or Pharmacology.
  • Three or more years of experience in a lab testing environment.
  • Experience in nonclinical toxicology.
  • Experience with in vitro assays.
  • Experience with flow cytometry.
  • Working knowledge of Good Laboratory Practices (GLP) regulations and study management.

Additional Skills & Qualifications

  • Ability to work cooperatively in a team environment.
  • Effective communication skills.
  • Strong problem-solving and troubleshooting abilities.
  • Ability to effectively prioritize and multitask.
  • Experience conducting effective meetings.
  • Ability to communicate effectively with staff and interface with both technical and non-technical personnel.
  • Understanding of Quality System Procedures and Test Methods.

Work EnvironmentThis position is based in both the lab and office, requiring onsite presence with no remote work option.Pay and BenefitsThe pay range for this position is $80000.00 – $90000.00/yr.Workplace TypeThis is a fully onsite position in Kitchener,ON.À propos d’Actalent:Actalent est un chef de file mondial des services d’ingénierie et de sciences et des solutions de talents. Nous aidons les entreprises visionnaires à faire progresser leurs initiatives en matière d’ingénierie et de science en leur donnant accès à des experts spécialisés qui favorisent la mise à l’échelle, l’innovation et la mise en marché rapide. Avec un réseau de près de 30 000 consultants et plus de 4 500 clients aux États-Unis, au Canada, en Asie et en Europe, Actalent est au service d’un grand nombre d’entreprises du classement Fortune 500.La diversité, l’équité et l’inclusionChez Actalent, la diversité et l’inclusion constituent le pont vers l’équité et la réussite de notre personnel. La diversité, l’équité et l’inclusion (DE&I) sont ancrées dans notre culture par :

  • L’embauche des talents diversifiés ;
  • Le maintien d’un environnement inclusif par une autoréflexion permanente ;
  • La mise en place d’une culture de soin, d’engagement, et de reconnaissance par des résultats concrets ;
  • L’assurance des opportunités de croissance pour nos gens.

Actalent est un employeur souscrivant au principe de l’égalité des chances et accepte toutes les candidatures sans tenir compte de la race, du sexe, de l’âge, de la couleur, de la religion, des origines nationales, du statut d’ancien combattant, d’un handicap, de l’orientation sexuelle, de l’identité sexuelle, des renseignements génétiques ou de toute autre caractéristique protégée par la loi.Si vous souhaitez faire une demande d’accommodement raisonnable, tel que la modification ou l’ajustement du processus de demande d’emploi ou d’entrevue à cause d’un handicap, veuillez envoyer un courriel à pour connaître d’autres options d’accommodement.About ActalentActalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.Diversity, Equity & InclusionAt Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I are embedded into our culture through:

  • Hiring diverse talent
  • Maintaining an inclusive environment through persistent self-reflection
  • Building a culture of care, engagement, and recognition with clear outcomes
  • Ensuring growth opportunities for our people

The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email for other accommodation options.

Global Study Manager, 12 Month Contract – AstraZeneca – Mississauga, ON

Company: AstraZeneca

Location: Mississauga, ON

Expected salary:

Job date: Wed, 22 Jan 2025 07:49:52 GMT

Job description: Global Study Manager, 12 Month Contract At AstraZeneca, we pride ourselves on crafting a collaborative culture…. specifications) You will support the Global Study Associate Director (GSAD) in project management as per agreed delegation…

Alexion Pharmaceuticals – Global Study Enablement Summer Student – Mississauga, ON

Company: Alexion Pharmaceuticals

Location: Mississauga, ON

Expected salary:

Job date: Sat, 11 Jan 2025 23:58:08 GMT

Job description: When we put unexpected teams in the same room, we fuel bold thinking with the power to inspire life-changing medicines. In-person working gives us the platform to connect, work at pace and challenge perceptions. That’s why we work, on average, a minimum of three days per week from the office. But that doesn’t mean we’re not flexible. We balance the expectation of being in the office while respecting individual flexibility. Join us in our unique and ambitious world.Our Canadian teamÂWe know that people living with a rare disease and their families deserve our unwavering commitment and investment into finding and accessing therapies that help them live longer, fuller lives. Our presence in Canada has grown to over 200 employees and includes a global research and development hub, made up of highly skilled professionals responsible for conducting our clinical trials in Canada and around the world, as well as our dedicated and hardworking local teams that ensures our treatments reach those who need them. Together, we are driving patient impact locally and globally.This role is a 4-month paid contract position, which starts in May 2025 and will end in August 2025. Our position will be based in our Mississauga head office and allow for flexible working arrangements working both onsite (3 times per week) and virtually.If you are interested in this position, please submit your resume. If you wish, you may also submit a cover letter indicating your interest and availability. There is no need to submit any additional documentation such as transcripts or marksheets.This is what you will do:The Global Study Summer Intern will be an integral part of the Global Study Enablement (GSE) team. In this role, they will support colleagues across the organization to accomplish business goals.You will be responsible for:

  • Complete assigned GSE tasks with guidance – Assist GSE team members in day-to-day work, such as maintaining and updating internal or study-related trackers, ensuring organization and accuracy.
  • Support study deliverables – Contribute to study and functional activities, including maintaining the study team roster, tracking study team training requirements, and ensuring timely updates.
  • Participate in process improvement initiatives – Collaborate on GSE team projects, such as enhancing workflows or supporting initiatives like the SME network, with mentorship and guidance.
  • Create, organize, and standardize GSE workspaces – Develop structured and efficient workspaces to facilitate collaboration and organization.
  • Track and present project activity progress – Regularly update the team on the status of assigned projects and contribute to ensuring deliverables are on track.
  • Engage in career development activities – Take part in one-on-one mentoring sessions focused on professional growth and exploring career opportunities.
  • Learn through meetings and training – Attend functional role-related meetings and therapeutic area training sessions, with a focus on gaining knowledge about rare diseases and clinical research.
  • Assist in study file reviews – Conduct periodic reviews of study files to ensure completeness, accuracy, and compliance with the scope of work and standard operating procedures.
  • Support clinical trial documentation tasks – Help with administrative and study-related responsibilities, including preparing, handling, distributing, filing, and archiving clinical trial documents.

Please note: Assignments and responsibilities may vary depending on project priorities and timing during the internship period.You will need to have:

  • Currently enrolled in a Bachelor’s degree program (or equivalent)
  • Strong communication skills – Ability to clearly and effectively convey information and project objectives across different teams, both in writing and verbally.
  • Proficiency in Microsoft Office Suite – Particularly in Excel, Word, and PowerPoint.
  • Familiarity with Microsoft Outlook – For scheduling meetings and managing email communications.
  • Proven ability to collaborate effectively – Experience working in team environments to achieve solutions-oriented results.
  • Keen attention to detail – Ensuring accuracy and thoroughness in tasks and deliverables.
  • Proactive mindset – Show initiative by offering creative ideas and solutions to contribute to project success.
  • Excellent organizational and time management skills – Capable of handling multiple priorities effectively within tight timelines.
  • Eagerness to learn – A genuine interest in clinical research and a desire to understand the regulatory requirements that govern this field.

We would prefer for you to have:

  • Experience with coding and data analytics – Familiarity with tools and programming languages is a plus, showcasing your ability to analyze and interpret data effectively.
  • Interest in pursuing a career in clinical research – A demonstrated passion for the field and a desire to grow within it, reflecting long-term commitment and enthusiasm.
  • Proficiency with specialized tools – Experience using Smartsheet and advanced features of Microsoft applications, such as PowerBi, is an asset.

What you will gain:

  • Knowledge of clinical trial operations and procedures.
  • An understanding of how study team’s function.
  • Professional development opportunities .
  • Exposure to various activities related to the phases of clinical trial research, therapeutic area and various branches of clinical trial settings.
  • Critical thinking skills related to operational aspects of a clinical trial, from design to start-up, through close.

At Alexion, you will find a collaborative culture that encourages innovation and a diverse environment where your contributions are valued. You will have the opportunity to be at the forefront of rare disease research and make a meaningful difference in patients’ lives.Alexion embraces diversity and equality of opportunity. We are committed to building an inclusive and diverse team representing all backgrounds, with as wide a range of perspectives as possible, and harnessing industry-leading skills. We believe that the more inclusive we are, the better our work will be. We welcome and consider applications to join our team from all qualified candidates, regardless of their characteristics. We follow all applicable laws and regulations on non-discrimination in employment (and recruitment), as well as work authorization and employment eligibility verification requirements.Ready to lead and inspire? Apply now and take the first step towards an exciting career at Alexion, AstraZeneca Rare Disease.AstraZeneca embraces diversity and equality of opportunity. We are committed to building an inclusive and diverse team representing all backgrounds, with as wide a range of perspectives as possible, and harnessing industry-leading skills. We believe that the more inclusive we are, the better our work will be. We welcome and consider applications to join our team from all qualified candidates, regardless of their characteristics. We comply with all applicable laws and regulations on non-discrimination in employment (and recruitment), as well as work authorization and employment eligibility verification requirements.

Associate Director, Evidence Project Management(Global Study Lead) – AstraZeneca – Mississauga, ON

Company: AstraZeneca

Location: Mississauga, ON

Expected salary:

Job date: Sat, 21 Dec 2024 04:11:44 GMT

Job description: and driving achievement of breakthroughs. Be primary AZ point of contact for the CRO Project Manager to secure study delivery… in and provide access to AstraZeneca therapies for patients in need. Associate Director, Evidence Project Management (AD EPM…

Senior Study Manager – Lycopodium – Vancouver, BC

Company: Lycopodium

Location: Vancouver, BC

Job description: professional engineering and project delivery services globally, across the resources, infrastructure and industrial processes… experienced and qualified Senior Study Manager to join and support our Vancouver based team to help enable our organic business…
A global company is seeking a Senior Study Manager to join their Vancouver team and support their engineering and project delivery services in resources, infrastructure, and industrial processes. The candidate should be experienced and qualified to contribute to the company’s organic growth.
Title: Account Manager – International Freight Forwarding

Location: Calgary, AB, Canada

Company: John G Russell (Transport) Ltd

Job Type: Full-time

Job Description:

John G Russell (Transport) Ltd is currently seeking an experienced Account Manager to join our team in Calgary, AB. The successful candidate will be responsible for managing and developing a portfolio of international freight forwarding accounts.

Responsibilities:
– Develop and maintain strong relationships with existing clients
– Actively seek new business opportunities and secure new accounts
– Understand clients’ needs and provide tailored solutions to meet their requirements
– Negotiate rates and service contracts with clients and suppliers
– Coordinate with operations teams to ensure smooth execution of shipments
– Monitor account performance and provide regular updates to clients
– Resolve any issues or concerns in a timely manner

Qualifications:
– Minimum of 3 years of experience in international freight forwarding sales/account management
– Proven track record of achieving sales targets and building client relationships
– Strong communication and negotiation skills
– Excellent problem-solving abilities
– Knowledge of industry trends and regulations
– Proficiency in Microsoft Office applications

If you are a motivated and results-driven individual with a passion for the logistics industry, we want to hear from you. Apply now to join our dynamic team at John G Russell (Transport) Ltd.

Expected salary:

Job date: Sun, 08 Dec 2024 07:39:08 GMT

Clinical Laboratory Study Manager – GlaxoSmithKline – Mississauga, ON

Company: GlaxoSmithKline

Location: Mississauga, ON

Expected salary:

Job date: Sun, 01 Dec 2024 01:40:38 GMT

Job description: compliance (ethical, legal, and regulatory) and quality to appropriate standards. The Laboratory Study Manager within HBSM-CT… is responsible for the operational setup & follow-up of central laboratory related activities for a project or a group of studies…

Associate Director, Evidence Project Management(Global Study Lead) – AstraZeneca – Mississauga, ON

Company: AstraZeneca

Location: Mississauga, ON

Expected salary:

Job date: Fri, 25 Oct 2024 22:42:43 GMT

Job description: . Be primary AZ point of contact for the CRO Project Manager to secure study delivery according to set criteria. Ensure the… for patients in need. Associate Director, Evidence Project Management (AD EPM) will lead the operational planning, delivery…

GlaxoSmithKline – Clinical Study Associate – Student Intern – Mississauga, ON

Company: GlaxoSmithKline

Location: Mississauga, ON

Expected salary:

Job date: Mon, 25 Nov 2024 01:38:14 GMT

Job description: Are you someone who is passionate and interested in a career at the pharmaceutical industry? Are you interested in clinical trials and how they make an impact on patient lives? If so, this internship may be the right opportunity for you!*Only candidates who have graduated within the last 2 years will be considered*This is a one-year contractJob Purpose:We are looking for collaborative, decisive, innovative team players to add value to Canada’s premier pharmaceutical company. If you are an energetic, career-minded professional with a passion for leadership, focus on solutions, and a commitment to outstanding performance, we invite you to apply to this exciting role.As a Clinical Study Associate Intern, you will be assisting Clinical Operations staff with the implementation and execution of clinical studies conducted in Canada across different therapy areas.Details (Your Responsibilities):This role will provide YOU the opportunity to learn about clinical trials and participate in key activities to progress your career; these responsibilities include, but not limited to the following:Complete various study related tasks for studies across oncology, vaccines and/or specialty care therapy areasBe involved in conducting site feasibility, including researching competitive landscape and collating feasibility results for new clinical trials in CanadaLiaise with investigative sites in the collection and processing of study related regulatory documentation.Assist with Canadianizing Informed Consent Forms for clinical studies.Assist with the review of various study specific documents.Assist with creating study newsletters, patient walk-throughs, and recruitment materials as required.Assist with preparation of study budgets.Assist with file reviews to ensure study documents are in audit ready state.Support the collection and conduct of management monitoring checks for various processes.Organize and coordinate operational therapy area team meetings.Assist with the conduct of on-site visits to ensure understanding of Good Clinical Practice (GCP) compliance, where applicableBe involved in site and study management including ensuring completion and delivery of all local activities required to ensure high quality set up, execution and completion of studies to agreed timelines and budget.Actively participate in various projects to support departmental activitiesWhy you?Basic Qualifications:University degree (within the past 2 years or less)This role requires a good understanding of scientific and medical information and an ability to apply this understanding to the conduct of clinical research activities.Reliability and punctuality (high level of professionalism)Effective time management skills. Ability to effectively manage multiple priorities and responsibilities of increasing scope and complexity.Excellent verbal and written communication skillsStrong interpersonal skillsStrong planning & organizational skills, and the ability to work efficiently and effectively in a dynamic environment.Strong research, time-management, and PC skillsAbility to quickly learn various databases.Ability to identify problems early and seek innovative solutions.Preferred Qualifications:Advanced scientific training in the basic sciences (Biology, Pharmacology, etc.) at the post graduate level (e.g. MSc)Specific training in clinical research would be an asset.Bilingualism (English / French)Why GSK?Uniting science, technology and talent to get ahead of disease together.GSK is a global biopharma company with a special purpose – to unite science, technology and talent to get ahead of disease together – so we can positively impact the health of billions of people and deliver stronger, more sustainable shareholder returns – as an organisation where people can thrive. We prevent and treat disease with vaccines, specialty and general medicines. We focus on the science of the immune system and the use of new platform and data technologies, investing in four core therapeutic areas (infectious diseases, HIV, respiratory/ immunology and oncology).Our success absolutely depends on our people. While getting ahead of disease together is about our ambition for patients and shareholders, it’s also about making GSK a place where people can thrive. We want GSK to be a place where people feel inspired, encouraged and challenged to be the best they can be. A place where they can be themselves – feeling welcome, valued, and included. Where they can keep growing and look after their wellbeing. So, if you share our ambition, join us at this exciting moment in our journey to get Ahead Together.GSK is an equal opportunity employer committed to diversity and inclusion. We welcome applications from all qualified individuals to apply to our career opportunities. GSK is committed to accommodating persons with disabilities. If you need accommodation at any stage of the application process or want more information on our accommodation policies, please contact us at . Please do not send resumes to this e-mail and instead apply through the online application process of this posting.Important notice to Employment businesses/ AgenciesGSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK’s commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.