Syneos Health, a leading global biopharmaceutical solutions organization, is actively hiring for three critical roles in India across Clinical Operations and Pharmacovigilance functions. These include:
- Clinical Resourcing Specialist – Hyderabad (Hybrid)
- Safety & PV Specialist I – Gurugram (Medical Device & PQC)
- Safety & PV Specialist I – Hyderabad/Gurugram (Medical Device & Product Quality)
These openings present strong opportunities for professionals seeking CRO jobs in India, pharmacovigilance specialist roles, and clinical resource management careers.
1️⃣ Clinical Resourcing Specialist – Hyderabad (Hybrid)
📍 Location: Hyderabad (Hybrid)
🕒 Experience: 1–2 years (Resource Management)
💼 Employment Type: Full-Time
Job Overview
The Clinical Resourcing Specialist job in Hyderabad focuses on workforce planning, analytics, resource allocation, and operational reporting within global clinical programs.
Key Responsibilities
- Manage daily STAT requests and resourcing workflows
- Analyze GRM export reports & budget validation reports
- Perform data QC and integrity checks
- Review Assigned & Available resource reports
- Support Just-In-Time (JIT) assignment processes
- Prepare presentations using Excel (Pivot tables, formulas) and PowerPoint
- Maintain SharePoint/Teams resourcing documentation
- Participate in cross-functional calls with Clinical Operations & BD teams
Required Qualifications
- BA/BS in Business, Management, Life Sciences, or Healthcare
- 1–2 years resource/logistics management experience
- CRO or pharmaceutical experience preferred
- Strong Excel & PowerPoint skills
- Ability to manage confidential workforce data
💰 Estimated Salary Range: ₹5,50,000 – ₹8,50,000 per annum
2️⃣ Safety & PV Specialist I – Medical Device & PQC (Gurugram)
📍 Location: Gurugram (Office-Based)
🕒 Experience: 2.5–4 Years
💼 Employment Type: Full-Time
Role Summary
This Pharmacovigilance Specialist job in Gurugram focuses on ICSR processing, Product Quality Complaint (PQC) case handling, and medical device safety reporting.
Core Responsibilities
ICSR Processing
- End-to-end case processing
- Medical coding using MedDRA
- Narrative writing & follow-up management
- Duplicate case identification
- Quality review of safety cases
Regulatory & Compliance
- Support expedited safety reporting
- xEVMPD validation & submission
- SPOR/IDMP compliance activities
- TMF & PSMF documentation
Required Qualifications
- B.Pharm / M.Pharm / PharmD / BDS / BMS / MBBS
- Minimum 1 year exclusive PQC handling
- Argus / ARISg database experience
- Knowledge of ICH-GCP, GVP & global PV regulations
💰 Estimated Salary Range: ₹6,00,000 – ₹9,50,000 per annum
3️⃣ Safety & PV Specialist I – Medical Device & Product Quality (Hyderabad/Gurugram)
📍 Location: Hyderabad / Gurugram
🕒 Experience: 2.5–4 Years
💼 Employment Type: Full-Time
Role Overview
This Safety & Pharmacovigilance Specialist job in India supports clinical trial and post-marketing safety operations including ICSR processing, regulatory submissions, and compliance oversight.
Key Responsibilities
- Perform end-to-end ICSR case processing
- Conduct quality review & compliance validation
- Medical coding (events, labs, medications)
- Support regulatory reporting timelines
- Maintain audit and inspection readiness
Required Qualifications
- B.Pharm / M.Pharm / PharmD / BDS / BMS / MBBS
- Experience in medical research safety cases
- Argus / ARISg hands-on experience
- Understanding of global drug & device safety regulations
💰 Estimated Salary Range: ₹6,00,000 – ₹9,50,000 per annum
Why Join Syneos Health?
- Exposure to global clinical trials & medical device safety programs
- Work with therapies across FDA & EMA markets
- Structured career growth in pharmacovigilance & clinical operations
- Global collaboration across 110 countries
- Inclusive and performance-driven culture
How to Apply
Application Link For Clinical Resourcing Specialist – Hyderabad (Hybrid)
Application Link For Safety & PV Specialist I – Medical Device & PQC (Gurugram)
