Medical Manager Lead- Immunology and Portfolio

Medical Manager Lead 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.

Principal Accountabilities

1. Develop and execute pre-launch to post-launch strategies/frameworks/tasks

• Develop and execute 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 accessibilities

2. Strategic stakeholder engagement

• As a credible and valued SME/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

3. 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.

4. 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

5. 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
• Mentor new colleagues and promote best-practice sharing to strengthen team capabilities and ensure high-quality medical engagement
• Support on the training and medical information activities for the field force

Requirements

• 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.
• 710 years of relevant experience in the pharmaceutical industry particularly in Medical Affairs or Clinical Research
• Fluency in English
• Medical/scientific expertise in Neurology and Immunology working knowledge of Regulatory Affairs Drug Safety Legal and Compliance and basic knowledge of Health Economics
• Knowledge of clinical operations and conduct of clinical trials would be an advantage.