Health Informatics jobs

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

Work Location: In person