NeuroHealth Sales Specialist – Orlando, FL – Teva Pharmaceuticals – Orlando, FL

Company: Teva Pharmaceuticals

Location: Orlando, FL

Expected salary:

Job date: Sat, 15 Feb 2025 02:42:09 GMT

Job description: The Marketing Director position at our specialty medicines business is a key role in driving growth and innovation through strategic research and development, business development, and marketing efforts. The ideal candidate will have demonstrated leadership and interpersonal skills, as well as a strong knowledge of reimbursement, managed care, or marketing principles. The Marketing Director will play a crucial role in driving the success of our business by developing and executing marketing strategies that position our products effectively in the market and drive growth and profitability. This role requires a proven track record of success in a similar capacity and a passion for driving innovation and growth in the pharmaceutical industry.

Vertex Pharmaceuticals – Patient Engagement Lead, Canada – Toronto, ON

Company: Vertex Pharmaceuticals

Location: Toronto, ON

Expected salary:

Job date: Thu, 06 Feb 2025 07:49:51 GMT

Job description: Job DescriptionThe Canadian Patient Engagement Lead (PEL), Senior Manager at Vertex Pharmaceuticals reports to the Senior Director, Public Affairs and Communications and is responsible for supporting the company’s Canadian patient engagement strategy across several functional areas. This position works closely with the Senior Director and the other Patient Engagement Senior Manager to help shape and drive the company’s ongoing efforts to build and sustain meaningful relationships and collaborations to support the needs of patients and advance our company’s goals.Job Responsibilities:· Work hand in hand with the Senior Director, Public Affairs and Communications and the other Patient Engagement Lead to execute the company’s patient advocacy strategy, including tactical implementation for current and future pipeline areas as appropriate· Serve as liaison between the patient community and VRTX; develop relationships with patient advocacy groups at the national and local levels to achieve Vertex goals, bring value to patients and enhance the Company’s standing and reputation· In collaboration with a cross functional team, identify policy priorities and barriers to access for patients; represent and advocate for the perspective of the patient communities in this work· Develop programming in partnership with the patient communities, including disease awareness and education· Ensure all activities are in line with legal and regulatory standards, as well as company policies and procedures, and adhere to Vertex’s standards of Integrity and Ethics· Attend all events and conferences working to build long-term, sustainable relationships with our patient advocacy groups (PAGs), support knowledge mobilization and clinical trial recruitmentJob Requirements:· Deep understanding of health decision-making and both national and local/regional access processes in Canada· Demonstrated experience as an appropriate partner to both the patient community and the Grants and Donations committee in effective and compliant management of the grants and donations process· Accurate financial management of allocated budgets· Ensure timely, appropriate and legally approved communications strategies· In partnership with communications team, integrate Vertex’s communications objectives with the patient advocacy strategy and identify additional communications opportunities where appropriate· Fulfilling other duties/projects as assignedMinimum Qualifications:· 5-7 years current and relevant experience in the pharmaceutical industry;· English (fluent) and French (working knowledge);· Bachelor’s degree required, advanced degree highly desired.Preferred Qualifications:· Demonstrates strengths in strategic planning, communication and presentation skills· Ability to travel (up to 25%) domestically and internationally· Pharmaceutical sector or non-profit sector and therapeutic area experience required· Ability to navigate seamlessly in a matrixed environment, able to work in situations with levels of ambiguity with independence· A high level of energy and passion toward patients, science and public health· Knowledge of the patient advocacy communities in our pipeline· Proven teamwork and collaboration skills, with a demonstrated ability to interact and influence all levels of business· Detail-oriented, self-initiating, well-organized and capable of managing multiple projects simultaneously· A desire to work in the corporate culture of a highly innovative company aimed at redefining health and transforming lives with new medicines#LI-BW1Flex Designation: Remote-EligibleFlex Eligibility Status:In this Hybrid-Eligible role, you can choose to be designated as:
1. Hybrid: work remotely up to two days per week; or select
2. On-Site: work five days per week on-site with ad hoc flexibility.Note: The Flex status for this position is subject to Vertex’s Policy on Flex @ Vertex Program and may be changed at any time.Company InformationVertex is a global biotechnology company that invests in scientific innovation.Vertex is committed to equal employment opportunity and non-discrimination for all employees and qualified applicants without regard to a person’s race, color, sex, gender identity or expression, age, religion, national origin, ancestry, ethnicity, disability, veteran status, genetic information, sexual orientation, marital status, or any characteristic protected under applicable law. Vertex is an E-Verify Employer in the United States. Vertex will make reasonable accommodations for qualified individuals with known disabilities, in accordance with applicable law.Any applicant requiring an accommodation in connection with the hiring process and/or to perform the essential functions of the position for which the applicant has applied should make a request to the recruiter or hiring manager, or contact Talent Acquisition at ApplicationAssistance@vrtx.com

Senior Manager, Regulatory Project Management – Alexion Pharmaceuticals – Mississauga, ON

Company: Alexion Pharmaceuticals

Location: Mississauga, ON

Expected salary:

Job date: Thu, 23 Jan 2025 23:46:12 GMT

Job description: Senior Manager, Regulatory Project Management When we put unexpected teams in the same room, we unleash bold thinking…. Join us in our unique and ambitious world. Â The Senior Manager, Regulatory Project Manager (RPM) is the RPM Lead for identified projects…

Area Business Manager – Central/South Florida – Madrigal Pharmaceuticals Corporation – Orlando, FL

Company: Madrigal Pharmaceuticals Corporation

Location: Orlando, FL

Expected salary: $140000 – 190000 per year

Job date: Wed, 15 Jan 2025 00:34:31 GMT

Job description: The Marketing Specialist in this position will be responsible for supporting a team of healthcare providers, including Endocrinologists and Advanced Practice Providers (APPs). They will analyze the utilization of sales and marketing tools and resources to ensure maximum effectiveness in reaching target audiences. This role requires a strong understanding of the healthcare industry, as well as the ability to collaborate with cross-functional teams to develop and implement successful marketing strategies. The Marketing Specialist will play a key role in driving patient engagement and positively impacting overall business outcomes for the healthcare providers they support.

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.

Business Intelligence Manager – Alexion Pharmaceuticals – Mississauga, ON

Company: Alexion Pharmaceuticals

Location: Mississauga, ON

Expected salary:

Job date: Sat, 04 Jan 2025 23:05:03 GMT

Job description: Introduction to role The Business Intelligence Manager is an exciting opportunity to be part of the Strategic Data… stakeholders. Must possess strong verbal and written communication skills – Excellent project management skills with demonstrated…

Global Meetings and Events Congress Project Manager – Alexion Pharmaceuticals – Mississauga, ON

Company: Alexion Pharmaceuticals

Location: Mississauga, ON

Expected salary:

Job date: Fri, 03 Jan 2025 23:32:28 GMT

Job description: disease strategies and improve care for patients with rare and devastating diseases. The Project Manager specializes in face… in the office while respecting individual flexibility. Join us in our unique and ambitious world. The Congress Project…

Thought Leader Liaison – North/Central Florida – Madrigal Pharmaceuticals Corporation – Orlando, FL

Company: Madrigal Pharmaceuticals Corporation

Location: Orlando, FL

Expected salary:

Job date: Sat, 28 Dec 2024 03:47:38 GMT

Job description: The ideal candidate for this role will have exceptional communication skills and a deep understanding of marketing principles. They will have experience in developing brand strategies and implementing innovative marketing tactics. This individual will be dedicated to advancing education, advocacy, and patient care within the field. Responsibilities include overseeing regional marketing initiatives, tracking progress on brand strategies, and informing the team on effective tactics to deploy. This role requires a passion for marketing, a commitment to excellence, and a drive to make a positive impact in the field.

Thought Leader Liaison – Florida – Madrigal Pharmaceuticals Corporation – Orlando, FL

Company: Madrigal Pharmaceuticals Corporation

Location: Orlando, FL

Expected salary:

Job date: Thu, 19 Dec 2024 05:33:50 GMT

Job description: We are seeking a highly skilled individual to take on the role of a Thought Leader Liaison for the Resmetirom brand. In this position, you will be responsible for building relationships and facilitating communication between influencers, advisers, healthcare providers involved in clinical trials, and local influencers who are aligned with our brand’s marketing needs.

The successful candidate will work closely with the HCP Marketing Team to plan and execute meetings and engagements that connect thought leaders with other relevant parts of the organization. This role requires excellent communication and networking skills, as well as a deep understanding of the healthcare industry and clinical trial processes.

If you are a strategic thinker, have a passion for building relationships, and are excited about being at the forefront of innovative healthcare solutions, we would love to hear from you. Join our team and help us drive the success of the Resmetirom brand through effective thought leader engagement.