Role & responsibilities

Review and summarize scientific literature, clinical trials, and treatment guidelines
Provide medico-scientific support for promotional and marketing materials
Respond to medical information queries from healthcare professionals and internal teams
Support the planning and execution of CMEs, advisory board meetings, and scientific events
Prepare product monographs, scientific dossiers, and clinical evidence summaries
Coordinate with the Pharmacovigilance team for adverse event reporting
Conduct scientific training programs for sales and field-force teams
Maintain an updated database of clinical publications, references, and competitor information

Preferred candidate profile

B.Pharm, M.Pharm, Pharm.D, BDS, BAMS, BHMS, MBBS,



or equivalent Life Sciences qualification 14 years of experience in Medical Affairs, Medical Writing, or Clinical Research Freshers with strong academic knowledge may also apply Solid understanding of pharmacology, clinical research, and evidence-based medicine Knowledge of pharmacovigilance principles and regulatory guidelines Excellent scientific writing and communication skills Proficiency in MS Office and literature databases such as PubMed and Google Scholar Ability to interpret and simplify complex clinical information for different audiences

📌 Medical Affairs Executive - Pharma (Chennai)
🏢 Phenom People
📍 Chennai