Safety Pharmacovigilance Specialist Jobs at Syneos Health. Apply for future PV roles in Hyderabad, Gurugram and Pune locations.
Introduction
Pharmacovigilance continues to be one of the most stable and high-demand career paths in the pharmaceutical and CRO industry. For professionals aiming to build or grow their careers in drug safety, this is a valuable opportunity. A globally recognized CRO is inviting applications for Safety & PV Specialist roles across India as part of its future hiring pipeline.
Company Overview
Syneos Health is a leading biopharmaceutical services organization that supports clinical development, medical affairs, and commercialization. The company collaborates with global pharma and biotech firms to accelerate drug development and ensure patient safety. With a presence in over 100 countries, it provides professionals with exposure to international pharmacovigilance systems and regulatory standards.
Job Overview
| Job Details | Information |
|---|---|
| Job Role | Safety & Pharmacovigilance Specialist |
| Company | Syneos Health |
| Location | Hyderabad / Gurugram / Pune |
| Experience | Freshers / Experienced |
| Qualification | Life Sciences / Pharmacy / Nursing |
| Employment Type | Full-Time (Hybrid) |
| Job ID | 25106956 |
| Hiring Type | Future Opportunity |
Job Location & Employment Type
- Locations: Hyderabad, Gurugram, Pune
- Work Mode: Hybrid (office + remote)
- Employment Type: Full-time
- Travel Requirement: As per project needs
Open Positions / Department Details
- Department: Pharmacovigilance / Drug Safety
- Role Level: Entry to Mid-level
- Hiring Type: Talent pipeline (future roles)
Key Roles & Responsibilities
As a Safety & PV Specialist, you will be responsible for managing drug safety data and ensuring compliance with regulatory standards. Your key responsibilities include:
- Processing Individual Case Safety Reports (ICSRs) as per SOPs
- Reviewing and validating safety data for accuracy and completeness
- Entering and managing data in pharmacovigilance databases
- Coding adverse events, medications, and medical history using MedDRA
- Preparing detailed case narratives and summaries
- Identifying missing information and following up for query resolution
- Supporting expedited reporting in compliance with regulatory timelines
- Conducting literature screening for safety-related information
- Handling duplicate case identification and management
- Supporting activities related to xEVMPD, SPOR, and IDMP
- Performing quality review of safety cases
- Ensuring proper documentation in TMF and safety files
- Participating in audits and maintaining compliance with global guidelines
Eligibility Criteria
Education
Candidates must have:
- Bachelor’s degree in Life Sciences
- Pharmacy graduate (B.Pharm / M.Pharm)
- Nursing or equivalent healthcare qualification
Experience
- Freshers and experienced candidates can apply
- Experience in pharmacovigilance or clinical safety is preferred
Skills Required
Candidates should demonstrate:
- Knowledge of pharmacovigilance processes and safety reporting
- Understanding of ICH-GCP, GVP, and regulatory requirements
- Familiarity with safety databases and medical terminology
- Knowledge of MedDRA coding
- Strong attention to detail and data accuracy
- Good communication and interpersonal skills
- Ability to manage multiple tasks and deadlines
- Proficiency in MS Office tools
- Ability to work independently and in team environments
Salary & Benefits
- Salary: As per company norms
- Hybrid work flexibility
- Exposure to global pharmacovigilance systems
- Career growth in drug safety and regulatory domains
- Training and development opportunities
- Collaborative and inclusive work culture
Selection Process
The hiring process may include:
- Resume screening
- Technical interview (PV concepts and case processing)
- HR discussion
- Final selection for future openings
How to Apply
Interested candidates can apply through the official careers portal of the company.
- Job ID: 25106956
- Apply online to be considered for upcoming roles
Important Dates
- Last Date: Not specified
- Note: This is a pipeline role for future hiring
Why Apply for This Pharma Job?
Pharmacovigilance is a critical function in ensuring drug safety and regulatory compliance. By applying for this opportunity, you can:
- Gain experience in global safety reporting systems
- Work on real-world adverse event case processing
- Build expertise in MedDRA coding and regulatory compliance
- Explore long-term career opportunities in drug safety
- Join a globally recognized CRO with strong industry presence
This role is ideal for candidates aiming to build a stable and rewarding career in pharmacovigilance.
Important Note / Disclaimer
IndiaPharmaJobs.in is an independent job information platform. We are not affiliated with Syneos Health or its recruitment team. We only provide job-related information for awareness purposes. Candidates should verify details independently before applying.
Final Call-to-Action
If you are interested in building or advancing your career in pharmacovigilance, this is a great opportunity to get shortlisted early. Apply now and stay ahead for upcoming openings in the drug safety domain.
