Fortrea Hiring Safety Science Coordinator I in Pune for pharmacovigilance, ICSR processing, safety reporting, and regulatory compliance roles.
Company Overview
Fortrea is a global clinical research organization specializing in clinical development, pharmacovigilance, and post-marketing safety services. The company supports pharmaceutical, biotechnology, and medical device organizations across the entire product lifecycle, with a strong focus on patient safety, regulatory compliance, and data integrity. Fortrea is recognized for its scientific expertise, robust quality systems, and commitment to delivering high-quality safety and regulatory solutions worldwide. Fortrea Hiring Safety Science Coordinator I
To strengthen its Patient Safety & Safety Science (PSS) operations, Fortrea is hiring a Safety Science Coordinator – I for its Pune location with a hybrid work model.
Job Location & Employment Type
- Location: Pune, Maharashtra, India
- Work Model: Hybrid (office and remote)
- Employment Type: Full-time
- Function: Pharmacovigilance / Patient Safety Services
- Role Level: Entry to early-career
Open Positions / Department Details
The Safety Science Coordinator – I role is part of Fortrea’s Clinical Safety / Patient Safety Services (PSS) team. This position supports both clinical trial and post-marketing safety activities, including the management of adverse events, expedited safety reporting, and regulatory submissions.
The role is suitable for candidates beginning or early in their pharmacovigilance careers who want exposure to ICSR processing, safety reporting, regulatory compliance, and quality systems. Fortrea Hiring Safety Science Coordinator I
Key Roles & Responsibilities
Selected candidates will support global safety operations under established procedures and timelines. Responsibilities include: Fortrea Hiring Safety Science Coordinator I
- Assisting with end-to-end processing of adverse events from clinical trials and post-marketing sources
- Supporting preparation and submission of Expedited Safety Reports (ESRs) and Periodic Safety Reports (PSRs)
- Maintaining adverse event tracking systems and project documentation files
- Logging and tracking all incoming AE/SAE reports accurately
- Entering safety data into safety databases in accordance with SOPs
- Drafting clear and medically consistent patient narratives
- Coding adverse events using MedDRA terminology
- Supporting listedness and expectedness assessments against product labels
- Generating follow-up queries for missing or inconsistent safety information
- Supporting timely submission of safety reports to clients, regulatory authorities, ethics committees, investigators, and partners
- Assisting with peer review, quality checks, and trend identification
- Supporting reconciliation of safety databases where applicable
- Maintaining country-specific adverse event reporting requirement files
- Working within Quality Management Systems, SOPs, and work instructions
- Supporting safety file archiving activities at study completion
- Coordinating internal and external meetings or teleconferences
- Training and mentoring junior safety staff or peers when required
- Providing administrative and operational support to PSS team members
- Ensuring compliance with regulatory, study-specific, and project-specific requirements
Fortrea Hiring Safety Science Coordinator I
Eligibility Criteria
Education
One of the following qualifications is acceptable:
- Non-degree qualification with 1–2 years of safety or relevant experience
- Associate degree with 6 months to 1 year of safety or relevant experience
- Bachelor’s degree (BS/BA) with 0–12 months of safety or relevant experience
- Master’s degree (MS/MA) with 0–6 months of safety or relevant experience
- PharmD with 0–6 months of safety experience
- One-year residency or fellowship may be considered relevant experience
Preferred disciplines:
Life Sciences, Pharmacy, Nursing, Medical Sciences, Biological Sciences, or related fields.
Experience
- Experience in adverse event or safety report processing is an advantage
- Relevant exposure in CRO, pharmaceutical, or biotech environments is beneficial
- Experience in related areas such as Clinical Data Management, Medical Affairs, Regulatory Affairs, or Quality Assurance may be considered
Skills Required
- Strong attention to detail and data accuracy
- Ability to prioritize tasks and manage multiple activities
- Good written and verbal communication skills
- Logical thinking and proofreading capability
- Basic numerical data handling skills
- Proficiency in MS Office and Windows applications
- Good keyboard and documentation skills
- Ability to work effectively within a team environment
- Fluency in English and local language (spoken and written)
Salary & Benefits
- Salary: As per company norms
- Benefits may include:
- Hybrid working flexibility
- Exposure to global pharmacovigilance projects
- Structured learning and safety training
- Career progression within patient safety and regulatory domains
- Statutory and company benefits as applicable
Fortrea Hiring Safety Science Coordinator I
Selection Process
- Online application screening
- Technical and functional interview
- HR discussion
- Final selection based on role suitability and compliance requirements
How to Apply
Interested candidates must apply online through Fortrea’s official careers portal before the closing time. Due to the urgent deadline, early application is strongly recommended.
Important Dates
- Application Deadline: 05 February 2026
Why Apply for This Pharma Job?
- Strong entry point into global pharmacovigilance operations
- Hands-on experience with safety reporting and regulatory compliance
- Opportunity to work with a reputed CRO on international projects
- Hybrid work model offering flexibility
- Long-term career growth in patient safety and clinical research
This role is ideal for candidates seeking to build a structured career in drug safety and pharmacovigilance. Fortrea Hiring Safety Science Coordinator I
Important Note / Disclaimer
IndiaPharmaJobs.in is an independent pharmaceutical job information platform and is not affiliated with Fortrea or any organization mentioned. Job details are shared for informational purposes only. Candidates should apply only through official company portals. No recruitment fees are charged for this role. Fortrea Hiring Safety Science Coordinator I
Final Call-to-Action
Eligible candidates should apply immediately to avoid missing this time-critical opportunity in pharmacovigilance and safety science. Fortrea Hiring Safety Science Coordinator I
