Fortrea has announced an opening for a Safety Science Coordinator-II in Bangalore, India. This is a full-time opportunity within the clinical safety and pharmacovigilance function, supporting safety activities for products across clinical trial and post-marketing settings.
The role involves processing adverse event reports, maintaining safety databases and tracking systems, preparing patient narratives, supporting expedited and periodic safety reporting, and ensuring that safety information is handled according to applicable regulatory and study-specific requirements.
Candidates with qualifications in Pharmacy, Life Sciences, Biological Sciences, Nursing, Medical Sciences or a related discipline may be eligible, depending on their educational level and relevant safety experience.
Fortrea Recruitment 2026 – Job Highlights
| Particulars | Details |
|---|---|
| Company | Fortrea |
| Job Title | Safety Science Coordinator-II |
| Job Requisition ID | 265159 |
| Job Location | Bangalore, India |
| Job Type | Full Time |
| Work Area | Clinical Safety / Pharmacovigilance |
| Experience | Varies by qualification; relevant safety experience required |
| Eligible Backgrounds | Pharmacy, Life Sciences, Biological Sciences, Nursing, Medical Sciences or related fields |
| Work Environment | Office or Remote |
| Application Deadline | October 8, 2026 |
| Salary / CTC | Not specified in the job posting |
About Fortrea
Fortrea is a global clinical research and healthcare services organization supporting pharmaceutical, biotechnology and medical technology companies with clinical development and related services.
The Safety Science function supports the management of safety information from clinical trials and post-marketing sources, helping clients meet applicable pharmacovigilance and regulatory requirements.
About the Safety Science Coordinator-II Role
The Safety Science Coordinator-II will support Clinical Safety and/or Pharmacovigilance and Safety Surveillance (PSS) activities.
A major part of the role involves receiving and processing adverse event reports from different sources, reviewing cases for completeness and accuracy, preparing safety documentation and ensuring that cases requiring expedited reporting are handled within the applicable timelines.
The position may support client projects as part of a wider project team or operate as a dedicated safety services function.
Key Responsibilities
The Safety Science Coordinator-II may be responsible for the following activities:
Adverse Event Processing
- Process adverse event reports according to client or sponsor requirements.
- Receive and manage safety reports originating from clinical trials and spontaneous or post-marketing sources.
- Enter safety information into relevant adverse event databases and tracking systems.
- Review cases for completeness, accuracy and suitability for expedited reporting.
- Identify clinically important information that is missing from an initial report.
- Generate follow-up queries to obtain additional information when required.
- Consult medical personnel when medical input is necessary.
- Ensure cases receive the appropriate level of medical review.
Medical Coding and Case Documentation
- Prepare patient narratives where required.
- Code adverse events accurately using MedDRA, when applicable.
- Assess cases against applicable product labeling requirements where relevant.
- Maintain accurate and complete safety case documentation.
- Ensure processed information meets the required quality standards.
Expedited Safety Reporting
- Identify cases requiring expedited reporting.
- Prioritize applicable safety cases according to regulatory and study-specific timelines.
- Support submission of expedited Serious Adverse Event (SAE) reports to appropriate recipients.
- Coordinate submissions to clients, regulatory authorities, ethics committees, investigators, vendors, partners and project personnel when required by the study plan.
- Support the processing and submission of Expedited Safety Reports (ESRs).
Periodic Safety Reporting
The role may also support Periodic Safety Reports (PSRs) and related activities, including:
- Maintaining safety reporting trackers.
- Supporting preparation and submission activities.
- Maintaining project-level documentation.
- Coordinating reporting activities within agreed timelines.
- Supporting communication with relevant project stakeholders.
Database Reconciliation and Quality Activities
- Assist with database reconciliation activities.
- Support quality and peer review of processed safety reports.
- Maintain study and project documentation according to agreed requirements.
- Monitor data quality and compliance with applicable procedures.
- Assist with quality issue management.
- Support audit and inspection preparation when required.
Team and Project Support
- Support training activities for PSS team members.
- Provide mentoring and peer support when required.
- Contribute information for monthly status reports.
- Assist with preparation and maintenance of PSS metrics.
- Support preparation for client meetings.
- Liaise with client contacts as appropriate.
- Perform additional responsibilities assigned by management.
Educational Qualification
Fortrea accepts multiple qualification and experience pathways for this position.
The job posting lists the following minimum pathways:
- Non-degree qualification plus 1 year of safety experience, or 3 years of relevant experience.
- Associate degree plus 1 year of safety experience, or 2 years of relevant experience.
- Bachelor’s degree plus 1 year of relevant experience.
- Master’s degree plus 1 year of relevant experience.
- PharmD plus 1 year of relevant experience.
- For PharmD candidates, a one-year residency or fellowship may be considered as relevant experience.
Preferred Educational Background
A degree in one or more of the following areas is preferred:
- Pharmacy
- Biological Sciences
- Life Sciences
- Nursing
- Medical Sciences
- Related scientific disciplines
Experience Requirements
Candidates should have relevant experience appropriate to their educational qualification.
The role particularly requires the ability to work accurately with safety information and regulated documentation. Experience in clinical safety, pharmacovigilance or related safety operations can be relevant to the position.
Required Skills
Fortrea highlights the following skills for the Safety Science Coordinator-II position:
- High level of accuracy
- Strong attention to detail
- Ability to work effectively as part of a team
- Willingness to provide peer support
- Good written communication
- Good verbal communication
- Ability to work independently with moderate supervision
- Good keyboard skills
- Familiarity with Microsoft Office
- Knowledge of Windows applications
- Mentoring skills are preferred
Pharmacovigilance and Regulatory Knowledge
Candidates should be able to understand and follow relevant safety-management procedures, including:
- Standard Operating Procedures (SOPs)
- Work Instructions (WIs)
- Pharmacovigilance procedures
- Safety reporting requirements
- Regulatory guidance
- Study and project-specific plans
- Applicable reporting timelines
The position requires adherence to governing regulatory requirements and responsibility for the quality of processed safety data.
Work Location and Work Environment
The job is based in Bangalore, India, and is listed as a full-time position.
The posting indicates that the work environment may be office-based or remote, depending on the role assignment and applicable arrangements.
Salary / CTC
Fortrea has not specified the salary or CTC for the Safety Science Coordinator-II position in the available job posting.
Candidates should confirm compensation details directly with Fortrea during the recruitment process.
Selection Process
The official job posting does not provide a detailed step-by-step selection process.
Candidates should follow the instructions provided through Fortrea’s official careers portal and be prepared to discuss their educational background, relevant safety experience, technical knowledge and communication skills during the recruitment process.
Application Deadline
The application deadline mentioned in the official posting is:
October 8, 2026
Candidates should verify the vacancy status before applying, particularly because the deadline is approaching.
How to Apply for Fortrea Recruitment 2026
Interested and eligible candidates can apply online through Fortrea’s official careers portal.
- Open the official Safety Science Coordinator-II vacancy.
- Review the qualification and experience requirements.
- Prepare an updated resume highlighting relevant safety, pharmacovigilance or clinical research experience.
- Complete the online application form.
- Submit the application before the stated deadline.
Official Application:
Important Details Before Applying
- Fortrea is hiring for the Safety Science Coordinator-II position.
- The job location is Bangalore.
- This is a full-time opportunity.
- Relevant safety experience is required, with the minimum varying according to the candidate’s qualification.
- Pharmacy, Life Sciences, Biological Sciences, Nursing and Medical Sciences are among the preferred educational backgrounds.
- Clinical safety or pharmacovigilance experience is relevant to the position.
- Knowledge of safety databases, adverse event processing and regulatory reporting can be useful for this role.
- MedDRA coding and patient narrative preparation are part of the listed responsibilities where applicable.
- The work arrangement may be office-based or remote depending on the assigned role.
- Salary/CTC has not been disclosed.
- The stated application deadline is October 8, 2026.
Frequently Asked Questions
1. What is the job title at Fortrea?
The position is Safety Science Coordinator-II.
2. Where is this Fortrea job located?
The vacancy is based in Bangalore, India.
3. What type of job is this?
It is a full-time position in the clinical safety and pharmacovigilance area.
4. What qualifications are accepted?
Fortrea lists multiple qualification pathways, including non-degree qualifications, associate degrees, bachelor’s degrees, master’s degrees and PharmD, subject to the specified relevant experience requirements.
5. Which educational backgrounds are preferred?
Preferred disciplines include Pharmacy, Biological Sciences, Life Sciences, Nursing and Medical Sciences or related fields.
6. Is prior safety experience required?
Relevant safety experience is required according to the qualification pathway specified in the job posting.
7. What does a Safety Science Coordinator-II do?
The role supports adverse event processing, safety data entry, medical coding, patient narratives, expedited reporting, periodic safety reporting, reconciliation, documentation, quality activities and client support.
8. Is MedDRA knowledge relevant to this job?
Yes. The job description includes accurate adverse event coding using MedDRA, where applicable.
9. Is the Fortrea Safety Science Coordinator-II position remote?
The posting lists the work environment as office or remote, depending on the role and applicable arrangement.
10. Has Fortrea announced the salary?
No. The available job posting does not specify the salary or CTC.
11. What is the last date to apply?
The stated application deadline is October 8, 2026.
12. Where can I apply for this vacancy?
Candidates can apply through Fortrea’s official careers portal using the application link provided in this article.
Important Note
This article has been rewritten from the information provided in the Fortrea job posting. Job availability, deadlines, eligibility criteria, work arrangements and recruitment requirements may change. Candidates should verify the latest information on Fortrea’s official careers portal before applying.