Fortrea Hiring 2026: Safety Science Coordinator – II Job in Bangalore
Fortrea is hiring for a Safety Science Coordinator – II position in Bangalore, India. The opportunity is focused on Clinical Safety and Pharmacovigilance (PSS) activities, including adverse event processing, safety data entry, MedDRA coding, patient narratives, regulatory reporting and safety database reconciliation.
The position is listed under requisition ID 265158 and offers an opportunity for professionals with relevant safety, pharmacovigilance or life-science experience to work within a global clinical research organization.
Fortrea provides safety and pharmacovigilance services across the product lifecycle, including clinical development and post-approval activities. Its official safety-services information specifically includes ICSR case processing, literature review, signal and risk management, safety database hosting and related patient-safety activities.
Fortrea Safety Science Coordinator II – Job Highlights
| Particular | Details |
|---|---|
| Company | Fortrea |
| Position | Safety Science Coordinator – II |
| Department | Clinical Safety / Pharmacovigilance |
| Location | Bangalore, India |
| Job Type | Full Time |
| Experience | 1+ years relevant Safety experience |
| Qualification | Relevant degree or equivalent experience |
| Requisition ID | 265158 |
| Application Deadline | September 21, 2026 |
| Work Area | Clinical Safety / Pharmacovigilance |
About Fortrea
Fortrea is a global contract research organization (CRO) supporting clinical development and healthcare research. Its operations span clinical development, patient safety and other services for biopharmaceutical and healthcare organizations.
The company’s careers information highlights opportunities for learning, collaboration and professional development across its global workforce.
Fortrea also operates dedicated safety services covering pharmacovigilance activities from early clinical development through post-approval. Its safety organization states that it processes more than one million individual case safety reports (ICSRs) annually and supports activities such as adverse-event intake, ICSR processing, medical writing, signal and risk management and safety database operations.
About the Safety Science Coordinator – II Role
The Safety Science Coordinator – II role supports clinical safety and pharmacovigilance operations.
The position involves handling safety information received from clinical trials and post-marketing sources. A major part of the work is ensuring that safety cases are accurately entered, reviewed, coded and processed according to applicable procedures and reporting requirements.
The role can involve coordination with medical reviewers, safety teams and other project stakeholders to ensure cases are handled within required timelines.
Key Responsibilities
1. Adverse Event Processing
The Safety Science Coordinator will process adverse event reports received from applicable sources according to client-specific plans and procedures.
This includes reviewing incoming safety information and entering relevant data into safety databases and tracking systems.
2. Safety Data Review
The position requires careful review of cases for:
- Completeness
- Accuracy
- Consistency
- Clinically significant information
- Expedited-reporting requirements
- Appropriate medical review
Attention to detail is particularly important because safety information must be handled accurately throughout the case-processing workflow.
3. Patient Narratives
The role includes preparing patient narratives based on available clinical information.
Candidates may need to organize relevant medical information into a clear narrative while ensuring that the case documentation accurately reflects the available source information.
4. MedDRA Coding
The Safety Science Coordinator – II position involves MedDRA coding of adverse events.
Knowledge of medical terminology and pharmacovigilance case-processing concepts can therefore be useful for professionals applying for this role.
5. Missing Information and Queries
The role includes identifying missing or clinically important information within safety cases.
Where additional information is required, the coordinator may generate appropriate queries to obtain the necessary details.
6. Expedited Reporting
Safety cases requiring expedited reporting need to be prioritized and submitted within applicable regulatory timelines.
The role therefore requires good organization, timeline management and awareness of pharmacovigilance reporting procedures.
7. Quality and Peer Review
The position also supports quality-related activities, including peer review of processed safety reports.
This helps ensure that safety cases meet applicable quality requirements before completion or submission.
8. Reconciliation and Documentation
Additional responsibilities include supporting:
- Safety database reconciliation
- Project documentation
- Study-level documentation
- Tracking activities
- Quality review
- Process-related records
The role may also support training and mentoring activities for PSS staff when required.
Eligibility Criteria
The source listing identifies 1+ years of relevant Safety or related experience, with requirements potentially varying according to educational background.
Relevant educational backgrounds include:
- Biological Sciences
- Pharmacy
- Nursing
- Medical Sciences
- Life Sciences
- Related scientific disciplines
The listing also indicates that candidates with relevant equivalent experience may be considered depending on their background.
Skills Required
Candidates applying for this position should have a combination of scientific knowledge, pharmacovigilance understanding and strong documentation skills.
Important skills include:
- Pharmacovigilance fundamentals
- Adverse event processing
- Safety data entry
- MedDRA coding
- Patient narrative writing
- Safety case review
- Knowledge of SOPs
- Understanding of work instructions
- Regulatory reporting awareness
- Strong attention to detail
- Written communication
- Verbal communication
- Team collaboration
- Ability to work independently
- MS Office knowledge
- Windows-based applications
Mentoring or peer-support experience can also be useful for the position.
Experience in Pharmacovigilance
Candidates with previous experience in clinical safety, pharmacovigilance, adverse event processing or safety data management may find their experience particularly relevant to this role.
Fortrea’s safety organization works across clinical and post-approval safety activities, including ICSR processing and safety database operations.
Applicants should clearly mention relevant safety systems, case-processing experience, MedDRA knowledge and regulatory reporting exposure on their resumes where applicable.
Work Location
Location: Bangalore, India
Job Type: Full Time
The source listing describes the position as an office or remote-preferred opportunity. Candidates should confirm the current working arrangement and applicable location requirements directly through the official application page before applying.
Application Deadline
According to the job information provided for this opening, the application deadline is:
September 21, 2026
Candidates should apply as early as possible and verify the current status of the vacancy on Fortrea’s official careers platform.
Requisition ID
Requisition ID: 265158
Using the requisition ID can help candidates identify the correct vacancy when searching through Fortrea’s career opportunities.
How to Apply for Fortrea Safety Science Coordinator II Job
Interested candidates should apply through the official Fortrea careers platform.
Position: Safety Science Coordinator – II
Location: Bangalore
Requisition ID: 265158
Apply for Safety Science Coordinator – II at Fortrea
Fortrea advises candidates to use its official career channels for genuine job opportunities. The company also warns applicants about recruitment fraud and states that legitimate openings are posted through its official career websites.
Resume Tips for Pharmacovigilance Candidates
Before applying, candidates can tailor their resumes to the requirements of the position.
Highlight Safety Experience
Mention experience related to:
- Adverse event processing
- ICSR case processing
- Clinical safety
- Pharmacovigilance
- Post-marketing safety
- Safety database management
Mention Technical Skills
Where applicable, include:
- MedDRA
- Safety databases
- Case processing
- Medical coding
- Narrative writing
- Reconciliation
- Regulatory reporting
Show Quality-Focused Experience
Candidates should also mention experience with:
- SOPs
- Work instructions
- Quality checks
- Peer review
- Case reconciliation
- Regulatory timelines
- Documentation
Why This Role May Interest Pharmacovigilance Professionals
This position brings together several core areas of pharmacovigilance, including safety case processing, medical coding, narratives, regulatory reporting and quality review.
Fortrea’s broader safety-services organization works across clinical and post-approval patient-safety activities, providing exposure to different areas of pharmacovigilance operations.
Fortrea’s careers platform also describes learning, collaboration and professional development as part of its employee experience.
Quick Job Summary
| Job Detail | Information |
|---|---|
| Company | Fortrea |
| Job Title | Safety Science Coordinator – II |
| Location | Bangalore |
| Department | Clinical Safety / Pharmacovigilance |
| Experience | 1+ years relevant Safety experience |
| Education | Biological Sciences, Pharmacy, Nursing, Medical Sciences, Life Sciences or equivalent |
| Job Type | Full Time |
| Requisition ID | 265158 |
| Deadline | September 21, 2026 |
| Core Skills | AE Processing, MedDRA, Narratives, Safety Data, Regulatory Reporting |
Frequently Asked Questions
Q1. What position is Fortrea hiring for in Bangalore?
Fortrea is hiring for a Safety Science Coordinator – II position in Bangalore.
Q2. What department does this role belong to?
The role is associated with Clinical Safety and Pharmacovigilance/PSS operations.
Q3. What experience is required?
The supplied job information specifies 1+ years of relevant Safety or related experience, with requirements varying according to educational background.
Q4. What qualifications are relevant for this position?
Relevant backgrounds include Biological Sciences, Pharmacy, Nursing, Medical Sciences and Life Sciences, along with equivalent relevant experience where applicable.
Q5. Does this role involve adverse event processing?
Yes. Processing adverse event reports from clinical and other applicable sources is a central responsibility of the role.
Q6. Is MedDRA knowledge required?
The job information identifies familiarity with MedDRA coding as a relevant skill for the position.
Q7. Does the position involve writing patient narratives?
Yes. Preparing patient narratives is included among the responsibilities.
Q8. Does the role involve regulatory reporting?
Yes. The position includes prioritizing and submitting expedited safety reports within applicable regulatory timelines.
Q9. What is the requisition ID?
The requisition ID is 265158.
Q10. What is the application deadline?
The supplied job information lists September 21, 2026 as the application deadline. Candidates should confirm the current vacancy status on the official Fortrea careers portal.
Q11. Where should candidates apply?
Candidates should apply through the official Fortrea career platform rather than through unofficial recruiters or third-party payment requests.
Q12. Does Fortrea provide pharmacovigilance services?
Yes. Fortrea’s official safety-services information describes end-to-end safety and pharmacovigilance services, including ICSR processing, literature review, signal and risk management and safety database operations.
Final Note
The Fortrea Safety Science Coordinator – II opening in Bangalore is centered on clinical safety and pharmacovigilance operations. The role covers adverse event processing, safety data entry, MedDRA coding, patient narratives, queries, expedited reporting, quality review and reconciliation.
Candidates with relevant pharmacovigilance, clinical safety, pharmacy, life-science or medical-science backgrounds should review the complete requirements and apply through Fortrea’s official careers platform before the stated deadline.
