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 specialists 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.

Pay: ₹30,000.00 - ₹55,000.00 per month

Perks:
Health insurance
Provident Fund

Work Location: In person

📌 Drug Safety Associate Surat (India)
🏢 Refined Reports Data
📍 India