Senior Drug Safety Associate

3 days ago


Remote, India beBeePharmacovigilance Full time ₹ 1,04,000 - ₹ 1,30,878

Pharmacovigilance Specialist


In this challenging role, you will play a key part in ensuring the safety of patients by reviewing and processing safety events for both pre-marketing and post-marketing products. You will also analyze abstracts and full articles to extract safety information and generate data listings from the safety database.

Key Responsibilities:
  • Review and process safety events according to assigned tasks and project-specific procedures.
  • Analyze abstracts and full articles to extract safety information for both pre and post-marketed products.
  • Generate data listings from the safety database, ensuring data accuracy.
  • Complete adverse event follow-ups via writing and/or phone, tailored to client requirements.
  • Maintain and review relevant safety tracking systems for accuracy and quality, assisting with project file maintenance.
  • Perform safety reviews of clinical and diagnostic data as part of case processing.
  • Develop and maintain the Safety Management Plan, ensuring project consistency.
  • Support post-marketing safety activities, including PSMF, RMP, and PBRER.
  • Liaise with investigational sites, reporters, and sponsors regarding safety issues.
Additional Requirements:
  • Experience in a pharmaceutical or CRO environment.
  • At least 1 year of experience in pharmacovigilance.
  • Excellent verbal and written communication skills.
  • Detail-oriented with strong organizational and time management abilities.
  • Fluent in written and verbal English.

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