Drug Safety Associate Job in Hyderabad Pharmacovigilance Role at TheReqrootr with 2 to 4 years experience apply now immediate joining opportunity
Grow Your Career in Pharmacovigilance & Drug Safety Operations
If you have hands-on experience in pharmacovigilance and case processing, this opportunity can help you advance in global drug safety operations. A clinical services organization is hiring Drug Safety Associates in Hyderabad, offering exposure to post-marketing surveillance, safety databases, and international regulatory systems.
Company Overview
TheReqrootr is facilitating hiring for a clinical services organization specializing in pharmacovigilance, clinical research, and regulatory services. The company supports global pharmaceutical clients in ensuring drug safety, compliance, and efficient clinical operations.
Job Overview (Quick Details)
| Field | Details |
|---|---|
| Job Title | Drug Safety Associate (Pharmacovigilance) |
| Company | Hiring via TheReqrootr (Client Organization) |
| Location | Hyderabad (Jubilee Hills) |
| Department | Pharmacovigilance / Drug Safety |
| Employment Type | Full-Time |
| Experience Required | 2–4 Years |
| Qualification | B.Pharm, M.Pharm, Pharm.D, BSc, MSc (Life Sciences) |
| Salary | ₹4.5 LPA – ₹7.5 LPA (Estimated) |
| Interview Mode | Face-to-Face |
Open Positions / Department Details
This position is part of the Pharmacovigilance (PV) and Drug Safety team. The role focuses on end-to-end case processing, post-marketing surveillance, and compliance with global safety regulations.
Candidates with experience in safety databases and regulatory reporting systems will find this role highly relevant.
Key Roles & Responsibilities
As a Drug Safety Associate, your responsibilities will include:
- Perform end-to-end Individual Case Safety Report (ICSR) processing
- Conduct post-marketing surveillance (PMS) activities
- Work on safety databases such as ArisG for case entry and workflow management
- Handle EudraVigilance submissions and reporting requirements
- Generate and validate XML files (E2B R2 / R3 formats)
- Ensure data accuracy, consistency, and regulatory compliance
- Collaborate with cross-functional teams in clinical safety operations
- Maintain proper documentation and follow global pharmacovigilance standards
Eligibility Criteria
Education
- B.Pharm / M.Pharm / Pharm.D
- BSc / MSc (Life Sciences)
Experience
- 2 to 4 years of experience in Pharmacovigilance
- Experience in case processing and safety database handling is required
Skills Required
Technical Skills:
- Strong knowledge of ICSR case processing and narrative writing
- Hands-on experience with safety databases (ArisG preferred)
- Knowledge of EudraVigilance and XML file handling
- Understanding of GVP guidelines and regulatory compliance
Soft Skills:
- Good communication and analytical abilities
- Attention to detail and data accuracy
- Ability to work in a team and manage timelines
Salary & Benefits
- Salary Range: ₹4.5 LPA – ₹7.5 LPA (based on experience)
- Opportunity to work on global pharmacovigilance projects
- Exposure to clinical trial safety operations and regulatory systems
- Career growth in PV, regulatory affairs, and clinical research domains
Selection Process
The hiring process includes:
- Resume screening
- Face-to-face interview (mandatory)
- Final selection and onboarding
How to Apply
Interested candidates can apply via email:
📧 Send your updated CV to: Careers@thereqrootr.com
📌 Suggested Subject Line: Application for Drug Safety Associate – IndiaPharmaJobs.in
Important Dates
- Job Published On: March 29, 2026
- Joining Requirement: Immediate joiners preferred
- Application Deadline: Not specified
Why Apply for This Pharma Job?
This role offers strong career growth in pharmacovigilance and global drug safety operations. It is ideal for professionals looking to enhance their expertise in case processing and regulatory compliance.
Key advantages include:
- Work on real-world pharmacovigilance and safety cases
- Exposure to international regulatory systems like EudraVigilance
- Experience with advanced safety databases
- Opportunity to grow in clinical research, PV, and regulatory roles
- Build expertise in global drug safety standards
Important Note / Disclaimer
IndiaPharmaJobs.in is an independent job information platform and is not affiliated with TheReqrootr or any employer mentioned. Candidates are advised to verify all details from official sources before applying. We do not charge any fees for job postings or applications.
Final Call-to-Action
If you have experience in pharmacovigilance and are ready for your next career move, apply now. Take advantage of this opportunity to grow in global drug safety operations.
