Vizen Life Sciences is a leading player in the life sciences industry, specializing in innovative solutions for drug safety, pharmacovigilance, and clinical research. Headquartered in Hyderabad, India, our state-of-the-art facility at Kapil Towers, 10th Floor, Gachibowli, is designed to foster collaboration and excellence. We are committed to ensuring the highest standards in post-marketing surveillance and regulatory compliance, helping pharmaceutical companies navigate complex global markets.
At Vizen, we prioritize employee growth, offering a supportive work environment with opportunities for professional development in PV operations. Our team works on cutting-edge projects involving spontaneous cases, literature monitoring, and health authority cases, all powered by advanced tools like the ARGUS Safety Database. As a 100% work-from-office organization, we build strong team dynamics while contributing to safer healthcare worldwide. Vizen Life Sciences is more than a workplace—it’s a hub for drug safety professionals passionate about making a difference.
Job Description: Drug Safety Associate / PV
As a Drug Safety Associate in our pharmacovigilance team, you will play a crucial role in managing post-marketing surveillance activities. This position demands a thorough understanding of complete case handling processes, from initial book-in to detailed data entry and beyond. Here’s a breakdown of your key responsibilities:
- Handle Spontaneous, Literature, and Health Authority Cases: Perform end-to-end case processing in post-marketing surveillance, ensuring accuracy and timeliness in reporting adverse events.
- Book-In and Data Entry Expertise: Utilize your 1-3 years of experience to efficiently book-in cases and execute data entry using the ARGUS Safety Database, maintaining compliance with global regulatory standards.
- Database Management: Work hands-on with the ARGUS Safety Database for case intake, narrative writing, and quality checks to support drug safety monitoring.
- Collaboration and Reporting: Collaborate with cross-functional teams to generate reports and contribute to PV operations, including signal detection and risk management.
- Compliance and Quality: Adhere to SOPs (Standard Operating Procedures) for pharmacovigilance activities, ensuring all post-marketing data is audit-ready.
This is a full-time, 100% work-from-office role based in Hyderabad’s Gachibowli area, offering a competitive salary, benefits, and growth potential for drug safety experts. If you thrive in a fast-paced environment focused on pharmacovigilance and drug safety, this position is tailored for you.
Key Requirements
- 1-3 years of proven experience in book-in and data entry within pharmacovigilance.
- Strong background in post-marketing surveillance, including handling spontaneous cases, literature cases, and health authority cases.
- Hands-on proficiency with the ARGUS Safety Database is mandatory.
- Excellent attention to detail, analytical skills, and knowledge of regulatory guidelines (e.g., ICH, FDA).
- Bachelor’s degree in Pharmacy, Life Sciences, or a related field.
- Immediate joiners preferred for quick onboarding.
Vizen Life Sciences values diversity and encourages applications from drug safety associates with a passion for PV excellence.
How to Apply for Drug Safety Associate / PV Position
Ready to advance your career in pharmacovigilance? Applying is simple and straightforward:
- Update Your Resume: Highlight your experience in post-marketing surveillance, book-in, data entry, and the ARGUS Safety Database.
- Submit Your Application: Email your resume and a cover letter to Praveen Kumar, General Manager HR, at plotti@vizenlifesciences.com. Use the subject line: “Application for Drug Safety Associate / PV – [Your Name]”.
