Medical Lead
3 weeks ago
Key Responsibilities
- Strategic Support:Align with the country medical affairs strategy based on global objectives, local insights, and market conditions. Implement Medical Affairs activities effectively within the designated therapy area(s).
- Event Coordination:Organize scientific meetings, symposia, congresses, Continuous Medical Education (CME) events, and other medical or scientific exchange activities. Develop and execute engagement plans for customer-facing activities.
- Quality Response:Respond to enquiries promptly and in accordance with applicable standards. Develop response documents for frequently asked questions.
- Clinical Input:Provide medical and scientific input for clinical trials and research activities. Oversee and support clinical studies and non-interventional studies/Investigator Initiated Trials (IITs) within the therapeutic area.
- Material Review:Coordinate the review and approval of medical and promotional materials. Ensure materials from global or regional sources are tailored to local needs and comply with local guidelines.
- Cross-Functional Communication:Share medical insights with various internal groups, including Pharmacovigilance, Regulatory Affairs, Market Access, QA, Commercial, and Brand teams.
- Risk Management:Identify and assess risks, plan mitigation strategies, and monitor internal controls within the scope of responsibilities.
Essential Requirements
- Education:MBBS or MD is mandatory.
- Experience:Minimum of 1 year in the pharmaceutical industry.
- Skills:
- Operations Management and Project Execution
- Collaboration Across Boundaries
- Clinical Trial Design and Data Reporting
- Medical Science and Disease Area Knowledge
- Medical Education and Scientific Engagement
- Knowledge of Non-Interventional Studies (NIS) / Epidemiology Studies
- Medical Governance and Safety
Desirable Requirement
- Therapeutic Area Knowledge:Cardiovascular
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