Fortrea is hiring for the position of Safety Science Coordinator – II in Bangalore, India. This is a full-time opportunity within the clinical safety and pharmacovigilance function.
The role involves supporting Clinical Safety and/or Product Safety Surveillance (PSS) operations for products across clinical trial and post-marketing environments. The selected candidate will be responsible for processing adverse event reports, maintaining safety databases and tracking systems, preparing patient narratives, coding medical information, supporting expedited safety reporting, and ensuring compliance with applicable regulatory and study-specific timelines.
Candidates with backgrounds in Biological Sciences, Pharmacy, Nursing, Medical Sciences, Life Sciences, or related disciplines may be eligible. The vacancy accepts several educational and experience combinations, including relevant experience for non-degree and associate-degree candidates as well as specific pathways for bachelor’s, master’s, and PharmD graduates.
Application deadline: September 21, 2026.
Fortrea Recruitment 2026 – Job Highlights
| Particulars | Details |
|---|---|
| Company | Fortrea |
| Job Title | Safety Science Coordinator – II |
| Job Requisition ID | 265158 |
| Job Location | Bangalore, India |
| Employment Type | Full Time |
| Functional Area | Clinical Safety / Product Safety Surveillance |
| Work Environment | Office or Remote |
| Experience | Varies by qualification |
| Preferred Background | Biological Sciences, Pharmacy, Nursing, Medical Sciences, Life Sciences or related |
| Key Skills | Safety Case Processing, MedDRA, Pharmacovigilance, Safety Reporting |
| Application Deadline | September 21, 2026 |
| Salary / CTC | Not specified |
| Application Mode | Online |
About Fortrea
Fortrea is a global clinical research and healthcare services organization involved in supporting clinical development and related activities.
The Safety Science Coordinator – II position supports safety operations associated with clinical trials and post-marketing products. The work involves processing safety information and ensuring that applicable cases are handled according to client requirements, study plans, standard procedures, and regulatory timelines.
Job Description
The Safety Science Coordinator – II will assist with Clinical Safety and/or Product Safety Surveillance activities. The role covers the management and processing of adverse event information received from clinical trials and spontaneous or post-marketing sources.
The selected candidate will review safety reports, enter information into safety databases, identify missing clinically significant information, prepare queries, code adverse events using MedDRA, prepare patient narratives, and support medical review and regulatory submissions.
The position also involves quality review, database reconciliation, project documentation, training support, client communication, metrics, audit preparation, and compliance activities.
Educational Qualification
Fortrea provides multiple qualification pathways for this position.
Candidates may qualify through combinations such as:
- Non-degree qualification with 1 year of Safety experience, or 3 years of relevant experience
- Associate degree with 1 year of Safety experience, or 2 years of relevant experience
- Bachelor’s degree (BS/BA) with 1 year of relevant experience
- Master’s degree (MS/MA) with 1 year of relevant experience
- PharmD with 1 year of relevant experience
- For PharmD candidates, a one-year residency or fellowship may be considered as relevant experience
The preferred academic disciplines include:
- Biological Sciences
- Pharmacy
- Nursing
- Medical Sciences
- Life Sciences
- Related scientific disciplines
Experience Requirements
The required experience depends on the candidate’s educational background, as outlined above.
Candidates should also demonstrate:
- Strong accuracy and 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
- Basic computer and keyboard skills
- Familiarity with Microsoft Office and Windows applications
Mentoring skills are preferred.
Key Responsibilities
1. Adverse Event Processing
The selected candidate will process adverse event reports received from different sources according to client or sponsor requirements.
Responsibilities include:
- Receiving and processing adverse event reports.
- Handling safety reports originating from clinical trials.
- Processing spontaneous reports from applicable sources.
- Entering safety information into adverse event databases and tracking systems.
- Reviewing cases for completeness and accuracy.
- Assessing whether cases are appropriate for expedited reporting.
- Processing safety information according to study and client-specific procedures.
2. Medical Review and Case Assessment
The role includes activities related to the clinical review of safety cases.
The candidate may:
- Identify clinically important information missing from initial reports.
- Generate follow-up queries to obtain additional information.
- Consult medical staff when required.
- Ensure cases receive appropriate medical review.
- Assess information relevant to safety reporting requirements.
3. Medical Coding and Patient Narratives
The position involves accurate processing of medical information.
Responsibilities include:
- Coding adverse events using MedDRA, where applicable.
- Preparing patient narratives.
- Reviewing coded information for accuracy.
- Supporting appropriate assessment of safety information.
- Determining applicable lists against product labels for marketed products, where relevant.
4. Expedited Safety Reporting
The selected candidate will support cases requiring expedited reporting.
This includes:
- Prioritizing cases requiring expedited reporting.
- Processing cases within applicable regulatory or study-specific timelines.
- Supporting submissions to worldwide regulatory agencies when required.
- Supporting submissions to other designated recipients according to client agreements.
Potential recipients may include:
- Clients
- Regulatory Authorities
- Ethics Committees
- Investigators
- Third-party vendors
- Partners
- Fortrea project personnel
5. Expedited and Periodic Safety Reports
The role includes supporting the preparation and submission of:
- Expedited Safety Reports (ESRs)
- Periodic Safety Reports (PSRs)
Responsibilities may include:
- Maintaining reporting trackers.
- Supporting ESR and PSR preparation.
- Assisting with submissions within study-specific timelines.
- Maintaining associated documentation.
- Coordinating reporting activities with relevant stakeholders.
Safety Tracking and Documentation
The Safety Science Coordinator will support the maintenance of project-level safety documentation.
Activities may include:
- Maintaining tracking systems.
- Setting up project files.
- Maintaining central documentation files.
- Maintaining study/project-level records.
- Ensuring documentation follows agreed requirements.
- Supporting appropriate filing of safety-related information.
Quality Review and Database Reconciliation
Quality is an important part of safety case processing.
The candidate may:
- Support peer review of processed safety reports.
- Perform quality reviews where assigned.
- Assist with database reconciliation.
- Support related reconciliation activities.
- Maintain accuracy and integrity of processed safety data.
- Identify and address quality issues according to applicable procedures.
Training and Team Support
The role may also involve supporting the development of other team members.
Responsibilities include:
- Supporting training of Product Safety Surveillance staff.
- Providing peer assistance where required.
- Mentoring team members where appropriate.
- Supporting knowledge sharing within the team.
- Maintaining knowledge of applicable SOPs, work instructions, and safety procedures.
Metrics and Reporting
The selected candidate may contribute to operational reporting activities.
This can include:
- Providing input for monthly status reports.
- Supporting PSS metrics.
- Assisting with generation and maintenance of operational metrics.
- Providing accurate information for project-level reporting.
Client Communication
The position involves supporting client-facing activities when required.
The candidate may:
- Assist in preparing for client meetings.
- Support the preparation of relevant safety information.
- Liaise with client contacts where appropriate.
- Provide information related to assigned safety activities.
- Support communication between internal project teams and clients.
Audit and Inspection Support
The Safety Science Coordinator will support quality and compliance activities associated with audits and inspections.
Responsibilities may include:
- Supporting quality issue management.
- Assisting with audit preparation.
- Supporting inspection readiness activities.
- Maintaining appropriate safety documentation.
- Ensuring assigned activities comply with applicable requirements.
Regulatory and Compliance Requirements
The role requires an understanding of safety-management procedures and applicable regulatory requirements.
The selected candidate will be expected to follow:
- Applicable pharmacovigilance requirements
- Regulatory reporting requirements
- Fortrea SOPs
- Work Instructions
- Procedural and guidance documents
- Client-specific requirements
- Study/project plans
- Applicable safety reporting timelines
The candidate is also responsible for maintaining the quality and accuracy of processed safety data.
Required Skills
Technical Skills
- Adverse event processing
- Pharmacovigilance / Clinical Safety
- Safety case data entry
- MedDRA coding
- Safety reporting
- Safety database management
- Case tracking
- Database reconciliation
- Microsoft Office
- Windows applications
Professional Skills
- High attention to detail
- Accuracy in data processing
- Strong written communication
- Strong verbal communication
- Teamwork
- Peer support
- Independent working ability
- Time and task management
- Ability to work under moderate supervision
Mentoring skills are preferred.
Work Location and Environment
Location: Bangalore, India
The vacancy indicates that the role may be performed in an office environment or remotely.
The exact work arrangement applicable to an individual candidate should be confirmed during the recruitment process.
Salary / CTC
The salary or CTC for the Safety Science Coordinator – II position has not been specified in the provided vacancy information.
Candidates should confirm compensation and other employment terms directly through Fortrea’s recruitment process.
Selection Process
A detailed selection process has not been provided in the vacancy.
Candidates may be assessed on their educational background, safety/pharmacovigilance experience, adverse event processing knowledge, attention to detail, communication skills, and understanding of applicable safety procedures.
The actual recruitment stages should be confirmed by Fortrea.
How to Apply for Fortrea Recruitment 2026
Interested and eligible candidates can apply online through the official Fortrea careers portal.
Application Deadline: September 21, 2026
Candidates should complete the application before the stated closing date and provide accurate details regarding their qualifications and relevant experience.
Important Details Before Applying
- Position: Safety Science Coordinator – II
- Company: Fortrea
- Job ID: 265158
- Location: Bangalore
- Employment: Full Time
- Work environment: Office or Remote
- Functional area: Clinical Safety / Product Safety Surveillance
- PharmD candidates can qualify with 1 year of relevant experience
- A one-year PharmD residency/fellowship may be considered relevant experience.
- Relevant bachelor’s and master’s degree pathways are available.
- MedDRA coding and adverse event processing are key activities.
- Salary/CTC is not disclosed.
- Application deadline: September 21, 2026
Frequently Asked Questions
1. What is the job title at Fortrea?
The position is Safety Science Coordinator – II.
2. What is the Fortrea job ID?
The job requisition ID is 265158.
3. Where is the position located?
The listed location is Bangalore, India.
4. Is this a full-time position?
Yes. The vacancy is listed as Full Time.
5. Can PharmD candidates apply?
Yes. The qualification criteria specifically include PharmD with 1 year of relevant experience. A one-year residency or fellowship may also be considered relevant experience.
6. Which educational backgrounds are preferred?
Preferred disciplines include Biological Sciences, Pharmacy, Nursing, Medical Sciences, Life Sciences, or related fields.
7. What type of safety work is involved?
The role involves adverse event processing, safety data entry, medical coding, patient narratives, medical review support, expedited reporting, periodic safety reporting, reconciliation, and quality activities.
8. Is MedDRA knowledge relevant?
Yes. The responsibilities include accurate adverse-event coding using MedDRA, where applicable.
9. Can the job be performed remotely?
The vacancy indicates an office environment or remote work arrangement.
10. What is the last date to apply?
The stated application end date is September 21, 2026.
Important Note
Job requirements, vacancy status, deadlines, work arrangements, compensation, and employment conditions may change. Candidates should verify the latest information on the official Fortrea careers portal before applying. Meeting the listed criteria does not guarantee selection or employment.