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Drug Safety Associate

0 years

3 - 9 Lacs

Posted:2 weeks ago| Platform: SimplyHired logo

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Work Mode

On-site

Job Type

Full Time

Job Description

Responsibilities:

  • Monitor and evaluate adverse drug reactions (ADRs) from clinical trials and post-marketing surveillance.
  • Ensure compliance with regulatory guidelines for drug safety reporting.
  • Prepare and submit safety reports to regulatory authorities.
  • Collaborate with healthcare professionals to assess and manage drug-related risks.
  • Maintain and update safety databases with accurate information.

Key Skills:

  • Attention to Detail: Precision in analyzing and documenting safety data.
  • Regulatory Knowledge: Familiarity with FDA, EMA, and ICH-GCP guidelines.
  • Communication Skills: Ability to convey safety findings effectively.
  • Analytical Thinking: Assessing risks and identifying safety signals.
  • Team Collaboration: Working with cross-functional teams in pharmacovigilance.

Job Type: Full-time

Pay: ₹350,000.00 - ₹975,000.00 per year

Benefits:

  • Health insurance
  • Provident Fund

Schedule:

  • Day shift

Work Location: In person

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