Apply online for Syneos Health pharma jobs for freshers and experienced PV specialists with salary, eligibility and night shift job details.
Introduction
If you are an experienced pharmacovigilance professional looking for a senior-level role with global exposure, this opportunity at Syneos Health could be the right move. The company is hiring for the Sr Safety & PV Specialist (Night Shift) role across multiple Indian locations. This position is ideal for candidates with strong experience in ICSR processing, safety data management, and regulatory compliance.
Job Overview
| Details | Information |
|---|---|
| Job Title | Sr Safety & PV Specialist (Night Shift) |
| Company Name | Syneos Health |
| Location | Hyderabad, Gurugram, Pune |
| Employment Type | Full-Time |
| Department | Pharmacovigilance / Drug Safety |
| Experience Required | Minimum 6 Years |
| Education | B.Pharm / M.Pharm / BDS / BMS / MBBS |
| Salary | As per company norms |
Company Overview
Syneos Health is a globally recognized organization offering integrated clinical and commercial solutions to pharmaceutical and biotech companies. With strong expertise in drug development and safety monitoring, the company supports a large number of global clinical trials and regulatory submissions. Syneos Health promotes a collaborative and inclusive work culture focused on innovation and patient impact.
Job Location & Employment Type
- Locations: Hyderabad, Gurugram, Pune
- Employment Type: Full-Time (Office-Based)
- Shift: Night Shift (mandatory)
Candidates must be comfortable working in night shifts as per global project requirements.
Open Positions / Department Details
- Role: Senior Safety & PV Specialist
- Department: Pharmacovigilance (PV)
- Function: ICSR Processing, Safety Reporting, and Compliance
This role involves advanced-level responsibilities in drug safety operations and quality review.
Key Roles & Responsibilities
The Sr Safety & PV Specialist Syneos Health role includes:
- Process Individual Case Safety Reports (ICSRs) as per SOPs and safety plans
- Perform triage and evaluate ICSRs for completeness and regulatory reporting
- Enter and manage safety data in pharmacovigilance databases
- Code adverse events, medical history, medications, and tests using MedDRA
- Prepare detailed narrative summaries for safety cases
- Identify missing information and follow up on queries
- Generate accurate and timely expedited safety reports
- Perform literature screening and safety data review
- Maintain drug dictionaries and ensure proper coding
- Handle xEVMPD product record validation and submission
- Identify and manage duplicate safety cases
- Support SPOR / IDMP-related activities
- Conduct quality checks (QC) of ICSRs
- Ensure proper documentation in TMF and PV system master files
- Maintain compliance with GCP, ICH, and global regulatory guidelines
- Participate in audits and inspections
- Collaborate with cross-functional teams and stakeholders
Eligibility Criteria
Education
- B.Pharm / M.Pharm / BDS / BMS / MBBS
- (Note: BSc / MSc candidates are not eligible)
Experience
- Minimum 6 years of pharmacovigilance experience
- Strong hands-on experience in ICSR case processing and quality check (QC)
Skills Required
- Strong knowledge of pharmacovigilance processes and safety reporting
- Expertise in MedDRA coding and safety databases
- Understanding of global regulations (ICH, GCP, GVP)
- Excellent analytical and problem-solving skills
- Strong written and verbal communication skills
- Ability to manage multiple tasks and deadlines
- Experience in regulatory submissions and compliance
Salary & Benefits
- Salary: As per company norms
Additional benefits may include:
- Career growth opportunities in global PV projects
- Training and skill development programs
- Exposure to international regulatory systems
- Inclusive and collaborative work culture
Selection Process
The hiring process generally includes:
- Online application submission
- Resume screening
- Technical interview (ICSR & PV focus)
- HR discussion
- Final selection
How to Apply
Interested candidates can apply through the official Syneos Health careers portal. Ensure your resume highlights your experience in ICSR processing, quality review, and pharmacovigilance systems.
Important Dates
- Application Deadline: Not specified (apply early recommended)
Why Apply for This Job?
The Sr Safety & PV Specialist Syneos Health Jobs 2026 role is a great opportunity for experienced professionals in pharmacovigilance. Here’s why this job stands out:
- Work on global safety projects with a reputed CRO
- Gain advanced experience in ICSR processing and quality review
- Opportunity to work with international regulatory standards
- Strong career progression in drug safety and PV operations
- Exposure to cutting-edge pharmacovigilance systems
This role is ideal for candidates searching for senior pharmacovigilance jobs in India with strong career growth potential.
FAQs
1. What is the role of a Sr Safety & PV Specialist?
The role involves processing safety cases, performing quality checks, and ensuring compliance with pharmacovigilance regulations.
2. Is night shift mandatory for this role?
Yes, candidates must be comfortable working in night shifts.
3. What experience is required?
A minimum of 6 years of pharmacovigilance experience with ICSR processing is required.
4. What qualifications are eligible?
B.Pharm, M.Pharm, BDS, BMS, or MBBS candidates are eligible.
5. How can I apply for this job?
You can apply online through the official Syneos Health careers website.
Conclusion
The Sr Safety & PV Specialist Syneos Health Jobs 2026 opportunity is ideal for experienced pharmacovigilance professionals aiming for senior roles. With global exposure, advanced responsibilities, and strong career growth, this role can significantly enhance your professional journey. Apply now to secure your opportunity.
Disclaimer
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