Looking for Pharmacovigilance jobs in Hyderabad? QPS Bioserve is hiring experienced professionals for the position of Drug Safety Associate in Hyderabad. Candidates with experience in adverse event case processing, MedDRA coding, and ICSR management can apply for this exciting pharmacovigilance opportunity.
This Drug Safety Associate role is ideal for professionals seeking growth in global drug safety operations, regulatory submissions, and clinical safety case processing within a reputed CRO environment.
Author: Pharmabharat Editorial Team
Job Overview
| Details | Information |
|---|---|
| Job Title | Drug Safety Associate |
| Company | QPS Bioserve |
| Location | Hyderabad |
| Experience | 4โ8 Years |
| Job Type | Full-Time |
| Work Mode | Work From Office |
| Department | Pharmacovigilance / Drug Safety |
| Salary | โน5.5 LPA โ โน9 LPA (Estimated) |
| Openings | 1 |
Drug Safety Associate Job Responsibilities
The selected candidate will be responsible for end-to-end pharmacovigilance and drug safety activities including:
- Processing adverse event cases for clinical trials and post-marketed products
- Performing MedDRA coding and assessing seriousness and expectedness
- Managing ICSR case processing workflows
- Conducting follow-up activities for missing safety information
- Writing and reviewing case narratives
- Submitting reports to regulatory authorities within timelines
- Downloading safety cases from regulatory authority portals
- Supporting PV training material development and delivery
- Performing peer review checks for quality and consistency
- Identifying discrepancies and escalating concerns to PV leadership
- Maintaining knowledge of global pharmacovigilance regulations
Required Qualifications & Skills
Candidates applying for this Pharmacovigilance job in Hyderabad should possess:
- Bachelorโs or Masterโs degree in Pharmacy, Life Sciences, or related field
- 4โ8 years of Pharmacovigilance or Drug Safety experience
- Basic knowledge of global pharmacovigilance regulations
- Experience with MedDRA coding and adverse event processing
- Strong written and verbal communication skills
- Excellent organizational and multitasking abilities
- High attention to detail and quality compliance mindset
Why Join QPS Bioserve?
Working at QPS Bioserve offers professionals exposure to:
- Global pharmacovigilance operations
- Regulatory compliance and drug safety reporting
- Clinical trial and post-marketing surveillance activities
- Career growth in CRO and life sciences industry
- Collaborative learning environment with experienced PV teams
How to Apply
Interested and eligible candidates can apply directly by sending their updated CV to:
Email: hr@qpsbioserve.com
Candidates are advised to mention โApplication for Drug Safety Associate โ Pharmabharatโ in the email subject line.