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Job Description & How to Apply Below
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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