Position: Pharmacovigilance Associate
Location: Hyderabad, Telangana, India
Industry: Pharma/ Healthcare/ Clinical research
Experience: 3-4 years in drug safety within the pharmaceutical industry
Qualification: Bachelor’s degree in Pharmacy
Key Responsibilities:
- Drafting procedural documents (SOPs, Work Instructions)
- Training development and delivery
- Adverse event reporting and management
- Regulatory correspondences and compliance activities
- Supporting audits and inspections
Candidate Profile:
- Strong knowledge of global pharmacovigilance regulations (FDA, Health Canada, EU)
- Familiarity with ICH-GCP guidelines
- Proficiency in MS Office (Word, Excel, PowerPoint)
- Excellent communication skills for liaising with internal and external stakeholders
Additional Information:
- Application Deadline: 30th July 2024
This role requires someone with experience in drug safety operations, regulatory compliance, and the ability to manage multiple projects effectively. If you’re interested, it might be a good fit given your background in regulatory affairs and clinical research interests.