Apply for Safety Science Coordinator job at Fortrea Pune. Check eligibility, experience, pharmacovigilance role details and apply online before deadline now.
The Safety Science Coordinator Jobs at Fortrea 2026 offer a valuable opportunity for candidates with pharmacovigilance or clinical safety experience to advance their careers in drug safety operations. This role, based in Pune, is ideal for pharmacy and life sciences professionals with experience in adverse event processing, safety reporting, and regulatory compliance. If you are looking to grow in the pharmacovigilance domain, this position provides excellent exposure to global safety standards and clinical trial processes.
Job Overview
| Field | Details |
|---|---|
| Job Title | Safety Science Coordinator I |
| Company Name | Fortrea |
| Location | Pune, Maharashtra |
| Employment Type | Full-Time |
| Department | Pharmacovigilance / Clinical Safety |
| Experience Required | 2+ Years |
| Education | B.Pharm / M.Pharm / Pharm.D / Life Sciences |
| Salary | As per company norms |
Company Overview
Fortrea is a globally recognized Contract Research Organization (CRO) providing clinical development and safety services to pharmaceutical and biotechnology companies. With expertise in clinical trials, pharmacovigilance, and regulatory support, Fortrea offers a dynamic work environment and opportunities to work on international projects.
Job Location & Employment Type
- Location: Pune, Maharashtra
- Employment Type: Full-Time
- Work Mode: Office-based
Open Positions / Department Details
Safety Science Coordinator I – Pharmacovigilance Role
This role focuses on managing adverse event reporting, safety data processing, and ensuring compliance with global pharmacovigilance regulations.
Key Roles & Responsibilities
- Process and manage Adverse Event (AE) and Serious Adverse Event (SAE) reports
- Handle Expedited Safety Reports (ESRs) and Periodic Safety Reports (PSRs)
- Perform data entry into safety databases and maintain tracking systems
- Write patient safety narratives and perform MedDRA coding
- Conduct listedness and causality assessments (as applicable)
- Generate queries for missing or inconsistent safety data
- Submit safety reports to regulatory authorities, clients, and stakeholders
- Assist in database reconciliation and quality checks
- Maintain documentation and compliance with SOPs and regulatory guidelines
- Support audits, inspections, and archiving activities
- Coordinate meetings and support project teams
- Train and mentor junior team members
Eligibility Criteria
Education
- B.Pharm / M.Pharm / Pharm.D
- Life Sciences / Medical Sciences background
Experience
- Minimum 2+ years in pharmacovigilance or clinical safety
- Experience in AE/SAE processing and safety reporting
Skills Required
- Knowledge of pharmacovigilance and drug safety processes
- Familiarity with MedDRA coding and safety databases
- Understanding of global regulatory requirements
- Strong attention to detail and data accuracy
- Good communication and teamwork skills
- Ability to manage multiple tasks and meet deadlines
Salary & Benefits
- Salary: As per company norms
- Opportunity to work in global pharmacovigilance projects
- Career growth in clinical safety and drug safety domain
- Exposure to international regulatory standards
- Learning and development opportunities
- Professional work environment
Selection Process
The recruitment process typically includes:
- Resume screening
- Technical interview
- HR interview
- Final selection
How to Apply
Interested candidates can apply online through the official Fortrea careers portal.
Important:
- Last Date to Apply: April 8, 2026
Apply as soon as possible due to limited time.
Why Apply for This Job?
The Safety Science Coordinator Jobs at Fortrea 2026 offer strong career benefits:
- Work in a global CRO with strong industry reputation
- Gain expertise in pharmacovigilance and clinical safety
- Exposure to international safety reporting standards
- Opportunity to work on global clinical trials
- Career advancement in drug safety domain
This role is ideal for professionals looking to specialize in pharmacovigilance and regulatory safety operations.
FAQs
1. What qualification is required for this role?
Candidates must have B.Pharm, M.Pharm, Pharm.D, or Life Sciences background.
2. How much experience is required?
Minimum 2+ years of experience in pharmacovigilance or clinical safety.
3. What is the job location?
The job is based in Pune, Maharashtra.
4. What skills are important?
Knowledge of AE/SAE processing, MedDRA coding, and safety databases is essential.
5. What is the last date to apply?
The last date to apply is April 8, 2026.
Conclusion
The Safety Science Coordinator Jobs at Fortrea 2026 provide an excellent opportunity for experienced professionals to advance in pharmacovigilance and clinical safety. With global exposure, strong career growth, and involvement in safety reporting processes, this role is ideal for building a long-term career in the CRO and pharmaceutical industry. Apply now before the deadline.
Disclaimer
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