We are seeking enthusiastic and detail-oriented freshers for the position of Drug Safety Associate. As a key member of our pharmacovigilance team, you will play a crucial role in ensuring the safety and efficacy of pharmaceutical products. This entry-level position is an excellent opportunity for recent graduates to start their careers in the pharmaceutical industry and gain hands-on experience in drug safety and pharmacovigilance.
Adverse Event Reporting: Collect, process, and report adverse drug reactions (ADRs) and other safety-related information in compliance with regulatory requirements.
- Data Management: Maintain accurate and up-to-date records of drug safety data in safety databases.
Case Processing:
Assist in the assessment, classification, and documentation of individual case safety reports (ICSRs).Regulatory Compliance:
Ensure that all safety reporting activities comply with global regulatory requirements and company policies.Literature Review: Support the review of scientific literature to identify and report safety-related information.
- Communication: Liaise with healthcare professionals, patients, and other stakeholders to gather and clarify safety data.
Education: B.Pharm or M.Pharm degree (2024 or 2025 pass out only).
- Attention to Detail: Strong analytical skills with the ability to accurately process and document data.
Communication Skills:
Excellent written and verbal communication skills.Computer Proficiency:
Familiarity with MS Office Suite and the ability to learn and use pharmacovigilance software.* Basic understanding of pharmacovigilance principles.
- Knowledge of regulatory guidelines such as ICH, GVP, and FDA regulations.
Job Types: Full-time, Permanent, Fresher
Experience:
- total work: 1 year (Preferred)
Work Location: In person
