SME-Medical Safety

About the role

Serve as a subject matter expert in medical safety within a global pharmaceutical environment applying research and development knowledge to support safe and effective product development. Contribute to risk assessment safety data interpretation and medical review activities in a hybrid work model ensuring day shift engagement and strong collaboration across cross functional teams.

What you'll do

• Apply medical safety expertise to interpret clinical and nonclinical data from pharma research and development activities ensuring that emerging safety signals are…
• Perform structured medical safety assessments of individual and aggregate case data from clinical trials and postmarketing sources focusing on accurate evaluation of…
• Collaborate with cross functional teams in research and development to provide timely medical safety input on study protocols informed consent documents and safety…
• Review and refine safety related sections of core clinical and regulatory documents including risk management narratives and summary reports ensuring that medical…
• Support signal detection activities by analyzing safety trends preparing concise summaries of safety data and recommending follow up actions that promote continuous…

What you need

• 2–3 yrs of experience
• Pharmacovigilance
• Communication
• Clinical research
• Any graduate