🧪Pharmacovigilance & Clinical Operations Roles in India
🏢 About Syneos Health
Syneos Health® is a leading global biopharmaceutical solutions organization providing integrated clinical, commercial, and consulting services to pharmaceutical, biotechnology, and medical device companies worldwide.
Operating across 110+ countries, the company supports drug development, clinical trials, pharmacovigilance, and medical device safety programs across FDA, EMA, and global regulatory markets.
Syneos Health is recognized for accelerating clinical development timelines and delivering therapies to patients faster through innovative, data-driven solutions.
📌 Current Openings
- Clinical Resourcing Specialist – Hyderabad (Hybrid)
- Safety & PV Specialist I – Medical Device & PQC – Gurugram
- Safety & PV Specialist I – Product Quality – Hyderabad/Gurugram
These roles offer strong career growth opportunities in clinical operations, workforce planning, pharmacovigilance, and medical device safety.
1️⃣ Clinical Resourcing Specialist – Clinical Operations
Location: Hyderabad (Hybrid)
Experience: 1–2 years
Role Overview: This role supports workforce planning and resource allocation across global clinical programs, ensuring optimal staffing, utilization, and operational efficiency.
Key Responsibilities- Manage resourcing workflows and STAT requests
- Analyze GRM export reports and budget validation reports
- Perform data quality checks and resource availability reviews
- Support Just-In-Time (JIT) assignment processes
- Create dashboards and presentations using Excel & PowerPoint
- Maintain SharePoint & Teams documentation
- Collaborate with Clinical Operations & Business Development teams
Qualification: BA/BS in Business, Management, Life Sciences, or Healthcare
Skills: Advanced Excel, analytics, workforce planning
Salary: ₹5.5 – ₹8.5 LPA
2️⃣ Safety & PV Specialist I – Medical Device & PQC
Location: Gurugram
Experience: 2.5–4 Years
Role Overview: This role focuses on medical device vigilance and product quality complaint handling, ensuring regulatory compliance and patient safety.
Core Responsibilities- End-to-end ICSR case processing & triage
- Medical coding using MedDRA
- Narrative writing and follow-up management
- Duplicate case detection & quality review
- Support expedited safety reporting
- xEVMPD validation & submission
- SPOR/IDMP compliance support
- Maintain TMF & PSMF documentation
Qualification: B.Pharm / M.Pharm / PharmD / BDS / MBBS
Skills: Argus/ARISg, GVP guidelines, PQC handling
Salary: ₹6 – ₹9.5 LPA
3️⃣ Safety & PV Specialist I – Product Quality
Location: Hyderabad / Gurugram
Experience: 2.5–4 Years
Role Overview: Supports clinical trial safety and post-marketing surveillance activities, ensuring compliance with global pharmacovigilance regulations.
Key Responsibilities- End-to-end ICSR case processing
- Medical coding of events, labs & medications
- Quality review & compliance validation
- Support regulatory reporting timelines
- Maintain audit & inspection readiness
Qualification: B.Pharm / M.Pharm / PharmD / MBBS
Skills: Drug safety, compliance, global PV regulations
Salary: ₹6 – ₹9.5 LPA
🌍 Why Join Syneos Health?
- Work on global clinical trials & medical device safety programs
- Exposure to FDA, EMA & international regulatory frameworks
- Structured career growth in pharmacovigilance & clinical operations
- Opportunity to collaborate with global healthcare teams
- Inclusive and performance-driven work culture
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