Syneos Health is hiring for the position of Safety & PV Coordinator in Gurugram, India. The vacancy is listed as a full-time, office-based opportunity and is scheduled to accept applications until September 8, 2026.
The role is focused on pharmacovigilance and safety operations, including Individual Case Safety Report (ICSR) processing, safety database activities, medical coding, literature screening, quality review and regulatory reporting support. The position may be relevant to candidates looking to build or continue a career in pharmacovigilance and clinical safety operations.
Syneos Health Recruitment 2026 – Job Highlights
| Job Detail | Information |
|---|---|
| Company Name | Syneos Health |
| Job Title | Safety & PV Coordinator |
| Job ID / Requisition ID | 25112047 |
| Job Location | Gurugram, India |
| Work Mode | Office-based |
| Employment Type | Full time |
| Application Deadline | September 8, 2026 |
About the Company
Syneos Health is a life sciences services organization that works across drug development and commercialization. Its Clinical Solutions operations support pharmaceutical and healthcare-related programs through various clinical and safety services.
The company states that it has worked with 94% of novel FDA-approved drugs over the past five years and has supported studies involving thousands of sites and clinical trial patients.
Job Description
The Safety & PV Coordinator will support pharmacovigilance activities associated with clinical trials and post-marketing programs. The position involves handling safety information, processing ICSRs, maintaining safety records, performing medical and drug coding, and supporting regulatory reporting requirements.
The role also requires adherence to applicable Standard Operating Procedures (SOPs), safety plans, pharmacovigilance regulations and relevant clinical research guidelines.
Safety & PV Coordinator
The position involves coordinating and supporting safety case-processing activities from receipt and triage through data entry, coding, query follow-up, quality review and reporting. Depending on project requirements, the selected candidate may also contribute to literature screening, drug dictionary maintenance, xEVMPD activities, SPOR/IDMP-related work and audit support.
Eligibility / Educational Qualification
The available job information does not specify a particular degree, educational qualification or minimum years of experience for this position.
Syneos Health states that equivalent experience, skills and/or education may be considered, and the company determines what constitutes equivalent qualifications for the role.
Candidates should review the official vacancy information and assess their background against the responsibilities and regulatory knowledge expected for the position.
Skills and Qualifications
The role requires familiarity with or the ability to work with areas such as:
- Pharmacovigilance and safety reporting processes.
- Individual Case Safety Reports (ICSIs).
- Safety databases and case-processing activities.
- Medical coding and drug coding.
- MedDRA coding.
- Literature screening and safety-related literature review.
- Drug dictionary maintenance.
- ICSR quality review.
- Duplicate case identification and management.
- Regulatory reporting requirements.
- xEVMPD product record activities.
- SPOR and IDMP-related activities.
- Standard Operating Procedures and Work Instructions.
- Global drug, biologic and device regulations.
- Good Clinical Practice (GCP).
- ICH guidelines.
- Good Pharmacovigilance Practices (GVP).
- Clinical trial and post-marketing safety documentation requirements.
- Professional collaboration with internal and external project teams.
Key Responsibilities
The Safety & PV Coordinator may be responsible for:
- Entering information into pharmacovigilance quality and tracking systems for the receipt and tracking of ICSRs.
- Supporting ICSR processing according to applicable SOPs and project-specific safety plans.
- Triaging incoming ICSRs and checking case information for completeness and accuracy.
- Assessing whether available ICSR information meets applicable regulatory reporting requirements.
- Entering case information into the relevant safety database.
- Coding adverse events, medical history, concomitant medications and relevant tests.
- Preparing complete narrative summaries for safety cases.
- Identifying missing or unclear information that requires clarification.
- Raising queries and following up until the required information is received and satisfactorily resolved.
- Supporting timely and accurate preparation of expedited safety reports in accordance with applicable regulatory requirements.
- Maintaining safety tracking records for assigned activities.
- Conducting literature screening and safety-related literature reviews when required.
- Performing drug coding and supporting maintenance of the drug dictionary.
- Carrying out MedDRA coding activities as required.
- Validating and submitting xEVMPD product records, including appropriate coding of indication terms using MedDRA.
- Manually recoding product and substance terms that remain uncoded in ICSRs.
- Identifying and managing duplicate ICSRs.
- Supporting activities associated with SPOR and IDMP.
- Performing quality reviews of ICSRs.
- Ensuring relevant documents are filed in the Trial Master File (TMF) according to company SOPs and sponsor requirements for clinical trials.
- Supporting appropriate documentation within the Pharmacovigilance System Master File for post-marketing programs.
- Maintaining knowledge of applicable SOPs, Work Instructions, global safety regulations, GCP, ICH guidelines, GVP and project or program requirements.
- Developing professional working relationships with internal and external project team members.
- Participating in audits when required.
- Applying relevant safety-reporting regulatory intelligence to assigned safety activities.
Work Location and Shift Details
The position is based in Gurugram, India, and the vacancy is listed as Office-based.
The job is offered on a full-time basis. Specific working hours or shift timings have not been provided in the available job information.
Salary / CTC
Salary details have not been specified in the available job information. Candidates should refer to the official Syneos Health careers portal or employer communication for compensation details.
Selection Process
The job posting does not provide complete information about the selection process, interview rounds or assessment stages. Candidates should follow the recruitment instructions provided by Syneos Health during the application process.
Benefits / Career Opportunities
Syneos Health states that it supports employee development through career progression, line-management support, technical and therapeutic-area training, peer recognition and a total rewards program.
The company also describes an inclusive work culture and opportunities to collaborate with teams involved in life sciences and healthcare programs.
Specific benefits such as salary incentives, insurance, bonuses, transportation or other individual employment benefits have not been specified for this vacancy.
How to Apply
Candidates interested in the Safety & PV Coordinator position can apply through the official Syneos Health careers portal.
The Job Requisition ID is 25112047. Applicants should carefully review the vacancy requirements and submit complete and accurate information during the recruitment process.
The listed application deadline is September 8, 2026.
Important Details Before Applying
- Company: Syneos Health
- Position: Safety & PV Coordinator
- Location: Gurugram, India
- Qualification: Not specifically mentioned in the available job information
- Experience: Not specifically mentioned
- Job Type: Full time
- Work Mode: Office-based
- Job ID: 25112047
- Application Deadline: September 8, 2026
Important Note
Job availability, responsibilities, eligibility requirements and application deadlines may change. Candidates should verify the latest information on the employer’s official careers website before applying. Syneos Health also states that the responsibilities listed in the job description are not exhaustive and that additional duties may be assigned according to business requirements.
FAQs
Who can apply for the Syneos Health Safety & PV Coordinator job?
The available job information does not specify a particular educational qualification or minimum experience requirement. Candidates should evaluate their skills and experience against the pharmacovigilance responsibilities described in the vacancy.
What does a Safety & PV Coordinator do?
The role supports pharmacovigilance activities such as ICSR processing, case triage, safety database entry, medical and drug coding, query follow-up, quality review, literature screening and regulatory reporting activities.
Where is the Safety & PV Coordinator job located?
The position is based in Gurugram, India.
Is this a work-from-home position?
No. The vacancy is listed as Office-based, although specific working hours have not been provided.
What is the job requisition ID?
The Job Requisition ID for this position is 25112047.
What is the application deadline?
The listed application deadline is September 8, 2026. Candidates should verify the current status on the official Syneos Health careers portal before applying.