Vigilare Biopharma is a trusted name in the pharmaceutical industry, specializing in drug safety and pharmacovigilance services. With a commitment to patient safety and regulatory compliance, Vigilarebp.com offers cutting-edge solutions in adverse event reporting and drug safety monitoring. The company is dedicated to maintaining high-quality standards and supporting the global healthcare ecosystem.
Job Description: Drug Safety Associate (ICSR)
As a Drug Safety Associate at Vigilare Biopharma, you will play a crucial role in ensuring the safety of pharmaceutical products by processing and reviewing Individual Case Safety Reports (ICSRs). Your responsibilities will include:
- Pharmacovigilance Knowledge: Understanding the principles and practices of drug safety monitoring.
- MedDRA Coding: Accurately coding adverse events using the Medical Dictionary for Regulatory Activities (MedDRA).
- Literature Validity Assessment: Evaluating scientific literature for relevance and validity in safety reporting.
- ICSR Case Processing: Performing data entry and quality review of safety cases to ensure accuracy and compliance.
- Quality Review: Ensuring all case data meets regulatory and company standards.
Experience Required
- Freshers or candidates with 1-2 years of experience in pharmacovigilance or drug safety.
- Immediate joiners preferred.
Why Join Vigilare Biopharma?
- Opportunity to work with a reputed biopharma company.
- Gain hands-on experience in pharmacovigilance and drug safety.
- Work in a dynamic and supportive environment.
- Enhance your career growth in the pharmaceutical safety domain.
How to Apply
Interested candidates who meet the above criteria are encouraged to apply immediately. Please send your updated resume to hr@vigilarebp.com with the subject line: Drug Safety Associate.
