"Complete Success Guide for Pharma & Medical Students (2025-26)"
Are you passionate about ensuring drug safety and patient well-being? Vizen Life Sciences, a reputed name in pharmaceutical services, is hiring for Drug Safety Associate (DSA) and Pharmacovigilance (PV) professional roles in Hyderabad. This work-from-office opportunity is ideal for individuals with 1–3 years of experience in post-marketing surveillance, case processing, and ARGUS Safety Database operations.
Join a collaborative team dedicated to maintaining high safety standards and regulatory compliance in global drug safety management.
At Vizen Life Sciences, the selected candidates will play a crucial role in handling pharmacovigilance case processing and maintaining patient safety data. This includes managing adverse event reports, ensuring data accuracy, and supporting regulatory submissions as per global PV guidelines.
Interested professionals meeting the eligibility criteria can send their updated resume to:
Email: plotti@vizenlifesciences.com
Contact: Praveen Kumar (General Manager – HR) – +91 8008102515
Location: Gachibowli, Hyderabad
Experience Required: 1–3 years
1. Who can apply for Vizen Life Sciences pharmacovigilance jobs?
Candidates with 1–3 years of experience in drug safety, case processing, or ARGUS operations are eligible.
2. Is this a remote or office-based job?
This is a 100% work-from-office position located in Hyderabad, Telangana.
3. What tools are used for case management?
Candidates should be proficient in the ARGUS Safety Database for handling PV and AE cases.
If you’re a motivated professional with a background in pharmacovigilance and drug safety, this opportunity at Vizen Life Sciences can accelerate your pharma career. Apply today and become part of a team that contributes to global patient safety and regulatory excellence.
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