Apply for Safety & PV Specialist I at Syneos Health 2026. Check eligibility, salary, pharmacovigilance job details, and apply online.
Introduction
If you are aiming to build or advance your career in pharmacovigilance, this opportunity can be a strong fit. The Safety & PV Specialist I at Syneos Health role offers hands-on experience in drug safety operations, ICSR processing, and regulatory compliance. It is an excellent option for pharmacy and medical graduates seeking growth in the clinical safety and PV domain.
Job Overview
| Details | Information |
|---|---|
| Job Title | Safety & PV Specialist I |
| Company Name | Syneos Health |
| Location | Hyderabad / Gurugram / Pune |
| Employment Type | Full-Time |
| Department | Pharmacovigilance (PV) / Drug Safety |
| Experience Required | Minimum 2.6 Years |
| Education | B.Pharm / M.Pharm / BDS / BMS / MBBS |
| Salary | As per company standards |
Company Overview
Syneos Health is a globally recognized life sciences organization offering integrated clinical, medical, and commercial solutions. The company supports pharmaceutical innovation by providing expertise across drug development and post-marketing safety. With a strong global presence, Syneos Health plays a key role in ensuring drug safety and improving patient outcomes.
Job Location & Employment Type
- Location: Hyderabad, Gurugram, Pune (Office-based)
- Employment Type: Full-time
This is an on-site role where professionals will work closely with pharmacovigilance teams and global stakeholders.
Open Positions / Department Details
- Department: Pharmacovigilance / Drug Safety
- Role Focus: ICSR processing, safety data management, and regulatory compliance
- Level: Specialist I (with opportunities for progression to Specialist II)
Key Roles & Responsibilities
As a Safety & PV Specialist I Syneos Health job, your responsibilities will include:
- Processing and tracking Individual Case Safety Reports (ICSRs)
- Reviewing case data for completeness, accuracy, and regulatory compliance
- Entering and managing safety data in PV databases
- Coding adverse events, medications, and medical history using MedDRA
- Preparing detailed case narratives and documentation
- Identifying missing information and following up for query resolution
- Supporting expedited safety reporting as per regulatory guidelines
- Performing literature screening and safety data review
- Managing duplicate cases and ensuring accurate reporting
- Supporting xEVMPD submissions and product record validation
- Maintaining Trial Master File (TMF) and PV documentation
- Ensuring compliance with SOPs, GCP, ICH, and GVP guidelines
- Participating in audits and quality checks
- Collaborating with internal teams and external stakeholders
Eligibility Criteria
Education
- Required qualifications:
- B.Pharm / M.Pharm
- BDS / BMS
- MBBS
- Note: BSc / MSc candidates are not eligible
Experience
- Safety & PV Specialist I: Minimum 2.6 years
- (Higher roles may require 4+ years of experience)
Skills Required
- Strong understanding of pharmacovigilance processes
- Knowledge of ICSR handling and safety databases
- Familiarity with MedDRA coding and regulatory guidelines
- Understanding of GCP, ICH, and global safety regulations
- Attention to detail and data accuracy
- Analytical and problem-solving skills
- Good communication and teamwork abilities
- Ability to manage deadlines and multiple tasks
Salary & Benefits
- Salary: As per company standards
- Health and wellness benefits
- Career growth opportunities in pharmacovigilance
- Training and development programs
- Exposure to global drug safety projects
- Supportive and inclusive work environment
Selection Process
The recruitment process typically includes:
- Resume screening
- Technical interview (PV/domain knowledge)
- Managerial discussion
- HR round and final offer
How to Apply
Interested candidates should apply through the official Syneos Health careers portal (online application method).
Ensure your CV highlights your pharmacovigilance experience, ICSR handling, and regulatory knowledge.
Important Dates
- Application Deadline: Not specified (Apply early recommended)
Why Apply for This Job?
The Safety & PV Specialist I Syneos Health role offers strong advantages:
- Work with a globally reputed CRO in drug safety
- Gain hands-on experience in ICSR processing and regulatory reporting
- Opportunity to grow in pharmacovigilance and drug safety careers
- Exposure to international standards and global projects
- Stable and high-demand career path in the pharma industry
This role is ideal for candidates targeting pharmacovigilance jobs in India, drug safety roles, and CRO careers.
FAQs
1. Who can apply for this job?
Candidates with B.Pharm, M.Pharm, BDS, BMS, or MBBS and relevant PV experience can apply.
2. Is this a remote job?
No, this is an office-based role in Hyderabad, Gurugram, or Pune.
3. What is the required experience?
A minimum of 2.6 years of pharmacovigilance experience is required.
4. What skills are important for this role?
ICSR processing, MedDRA coding, safety database knowledge, and regulatory compliance skills are essential.
5. How can I apply for this job?
You can apply through the official Syneos Health careers portal online.
Conclusion
The Safety & PV Specialist I at Syneos Health 2026 is a great opportunity for professionals seeking to grow in pharmacovigilance and drug safety. With global exposure, structured career growth, and hands-on experience in safety reporting, this role can significantly strengthen your profile in the pharmaceutical industry. Apply early to secure your position.
Disclaimer
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