Key Responsibilities:

- Record and review adverse reactions in the safety database for post marketing and clinical trial reports in accordance with applicable regulatory standards, with high accuracy and quality.

- Assessment and review of literature abstracts and full-text articles.

- Communicate with required stakeholders, as necessary, to carry out the operational responsibilities.

- Carry out necessary administrative duties required for the job.

- Support effective functioning of PV projects (including but not limited to case processing,

- Literature Monitoring, Aggregate Reporting, Medical Writing, Signal Detection and

- Management, Medical Information and Risk Management etc.) in compliance with agreements and applicable regulations and guidelines.

- Have ownership of assigned projects and tasks and ensure adherence to timelines and quality.

- Management of quality, compliance and documentation across PV projects.

- Other responsibilities as assigned by the Management.

Education & Experience:

- B.Pharm / M.Pharm / BDS or equivalent qualification from a reputed institute recognized by Pharmacy Council of India

- 0-1 years of experience in drug safety/pharmacovigilance

📌 Drug Safety Associate - Clinical Safety and Pharmacovigilance (Noida)
🏢 Soterius
📍 Noida