Medical Manager– Immunology & Portfolio
Job Summary
Medical Manager for Immunology and Portfolio will lead from pre-launch to launch strategies development and medical activities for relevant pipelines and portfolios including Business Development assets. This person will be working in close collaborations with internal relevant functions (local and above country) and have peer-to-peer discussions with KMEs.
- Execute pre-launch to post-launch strategies/frameworks/tasks
- Support the development and execution of relevant medical activities eg. mappings or work closely with global counterparts to map out KMEs guidelines congress associations competitors
- Own the science and Medical from pre-launch to post-launch medical strategies and developments
- Collaborate with International and global teams for planning managing new studies and compassionate uses/Early Access Program at local level to accelerate patient accessibility
- Strategic stakeholder engagement
- As a credible and valued medical expert/partner to establish and maintain trusted scientific engagements with Key Medical Experts (KMEs) investigators and other stakeholders through scientific exchange as appropriate
- Coordinate and consolidate analysis and selection to define the KME universe for the country to identify and prioritize key experts for strategic engagement. Develop and execute KMEs engagement plan to support readiness activities
- Scientific and Clinical Support
- As SME to be updated with clinical knowledge published data and trial work for company products including attendance and collection of insights at scientific meetings and conferences
- Provide technical and educational support to internal local teams (e.g. Medical Affairs Drug Safety Medical Information Value & Market Access Regulatory Affairs Commercial) and healthcare professionals on Biogens disease areas and pipeline products including speaker support internal training and congress participation to ensure accurate and compliant dissemination of scientific knowledge.
- Evidence Generation and Research Collaboration
- Support Global clinical trial activities including site initiation and coordination in alignment with CCL; support Phase IV studies and registries set up to facilitate high-quality data generation and contribution to lifecycle management.
- Partner with appropriate study team members and CCSL for global studies as needed; influence country selection and/or lead site selection with coordinated input from appropriate stakeholders - as appropriate - for phase I-IV studies; support review of study documents including site visit reports and/or ICFs for global & local studies as needed
- Support Global clinical trial activities including site initiation and coordination in alignment with CCL; support Phase IV studies and registries set up to facilitate high-quality data generation and contribution to lifecycle management.
- Medical Education and Compliance
- Review scientific materials for accuracy and ensure compliance with local regulations to promote informed clinical decision-making and maintain Biogens ethical standards in medical communications
- Ensure accuracy of scientific responses to medical questions from HCPs and patients according to local law and internal regulations
- Support on the training and medical information activities for the field force
- Other job duties may be assigned. May be modified at any time as business needs required.
Qualifications:
- A medical degree (e.g. MD) or a natural science degree is required. An advanced terminal degree is preferred such as MD PhD or PharmD
- Candidates may also qualify with an equivalent combination of education and experience in relevant medical or scientific fields
- 57 years of relevant experience in the pharmaceutical industry
- 2-3 years of experience in Medical Affairs
- Fluency in and English
- Medical/scientific expertise in Immunology or Oncology or Ophthalmology working knowledge of Regulatory Affairs Drug Safety Legal and Compliance and basic knowledge of Health Economics
- Knowledge of medical affairs strategy in pipeline products would be an advantage
Why Biogen
We are a global team with a commitment to excellence and a pioneering spirit. As a mid-sized biotechnology company we provide the stability and resources of a well-established business while fostering an environment where individual contributions make a significant impact. Our team encompasses some of the most talented and passionate achievers who have unparalleled opportunities for learning growth and expanding their skills. Above all we work together to deliver life-changing medicines with every role playing a vital part in our mission. Caring Deeply. Achieving Excellence. Changing Lives.
At Biogen we are committed to building on our culture of inclusion and belonging that reflects the communities where we operate and the patients we serve. We know that diverse backgrounds cultures and perspectives make us a stronger and more innovative company and we are focused on building teams where every employee feels empowered and inspired.Read onto learn more about Biogen.
All qualified applicants will receive consideration for employment without regard to sex gender identity or expression sexual orientation marital status race color national origin ancestry ethnicity religion age veteran status disability genetic information or any other basis protected by federal state or local law. Biogen is an E-Verify Employer in the United States.
Required Experience:
Manager
About Company
Founded in 1978, Biogen is a leading biotechnology company that pioneers innovative science to deliver new medicines to transform patients lives and to create value for shareholders and our communities. We apply deep understanding of human biology and leverage different modalities, ... View more