Looking to grow your career in pharmacovigilance (PV) and drug safety? Syneos Health is hiring a Safety & PV Coordinator in Hyderabad for candidates with 1โ3 years of experience in spontaneous cases and PMS case processing. This is a strong opportunity for B.Pharm/M.Pharm graduates aiming to build expertise in ICSR processing, MedDRA coding, and global safety reporting within a leading biopharmaceutical solutions organization.
With increasing demand for pharmacovigilance jobs in India, this role offers hands-on exposure to post-marketing surveillance (PMS), regulatory compliance, and safety database systems like Argus and LSMV.
Job Overview
- Position: Safety & PV Coordinator
- Company: Syneos Health
- Location: Hyderabad (Office-based)
- Qualification: B.Pharm / M.Pharm
- Experience: 1โ3 years (Spontaneous cases & PMS)
- Employment Type: Full-time
- Notice Period: Immediate to 30โ40 days preferred
- Database: LSMV (preferred), Argus acceptable
Key Responsibilities
As a Safety & PV Coordinator, you will handle end-to-end pharmacovigilance activities, including:
- Processing and tracking Individual Case Safety Reports (ICSRs)
- Performing triage, data entry, and quality checks for safety cases
- Conducting MedDRA coding for adverse events and medical terms
- Preparing clinical narratives and follow-up queries
- Ensuring compliance with ICH-GCP, GVP, and global safety regulations
- Managing duplicate case identification and reconciliation
- Supporting xEVMPD submissions and SPOR/IDMP activities
- Performing literature screening and safety signal detection support
- Maintaining documentation in Trial Master File (TMF) and PV systems
- Assisting in audit readiness and regulatory inspections
Required Qualifications
- Educational Qualification: B.Pharm or M.Pharm (mandatory)
- Experience: Minimum 1 year in pharmacovigilance (PMS & spontaneous reporting)
- Strong understanding of:
- ICSR lifecycle and safety reporting
- MedDRA coding and drug dictionaries
- Clinical trial phases (IIโIV) and post-marketing safety
- Familiarity with Argus or LSMV safety databases
- Good communication, analytical, and documentation skills
- Proficiency in MS Office (Excel, Word, Outlook)
Preferred Skills
- Experience in duplicate management and case reconciliation
- Knowledge of xEVMPD, SPOR, IDMP standards
- Ability to manage multiple safety cases with high accuracy
- Strong attention to detail and compliance mindset
Salary & Benefits
- Estimated Salary Range: โน3.5 LPA โ โน6.5 LPA (based on experience)
- Career growth in global pharmacovigilance projects
- Exposure to FDA, EMA, and international regulatory frameworks
- Structured training and professional development programs
- Collaborative and inclusive work culture
Why Join Syneos Health?
Syneos Health is a globally recognized biopharmaceutical solutions organization operating in over 110 countries. The company has contributed to:
- 94% of novel FDA-approved drugs
- 95% of EMA-authorized products
- 200+ global clinical studies
This makes it an ideal workplace for professionals seeking long-term growth in drug safety and pharmacovigilance careers.
How to Apply
Interested candidates can apply using the official link or email:
- Email your CV to: anamika.jayprakash@syneoshealth.com
