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Vizen Life Sciences is actively seeking skilled Drug Safety Associates / PV professionals in Hyderabad. This 100% work-from-office role is ideal for candidates with 1-3 years of experience in post-marketing surveillance, spontaneous case handling, and data entry activities. If you have hands-on experience with the ARGUS Safety Database, this is your chance to join a dynamic team ensuring patient safety and regulatory compliance.
Key Responsibilities
- Manage end-to-end pharmacovigilance (PV) case processing including spontaneous, literature, and health authority cases.
- Perform book-in and data entry activities accurately and efficiently.
- Maintain ARGUS Safety Database with complete and accurate case documentation.
- Ensure compliance with local and global pharmacovigilance regulations.
- Collaborate with cross-functional teams to support safety reporting and regulatory submissions.
Qualifications & Skills
- Experience: 1-3 years in post-marketing surveillance / drug safety.
- Technical Skills: Proven hands-on experience with ARGUS Safety Database.
- Educational Background: B.Pharm, M.Pharm, Life Sciences, or related fields.
- Strong attention to detail and ability to handle multiple case types.
- Excellent communication and documentation skills.
Benefits
- Competitive salary package (INR 4-6 LPA, negotiable based on experience).
- Professional growth in pharmacovigilance and drug safety operations.
- Exposure to global regulatory practices and ARGUS database expertise.
- Collaborative and supportive office environment in Gachibowli, Hyderabad.
How to Apply
Interested candidates can reach out to:
Praveen Kumar – General Manager HR
📞 +91 800 810 2515
📧 plotti@vizenlifesciences.com
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