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-related operations.
The role involves processing and managing adverse event reports originating from clinical trials and post-marketing sources. The selected professional will support safety data entry, case review, MedDRA coding, patient narratives, expedited reporting, safety report submissions, database reconciliation, quality review and pharmacovigilance compliance activities.
Candidates with qualifications in Biological Sciences, Pharmacy, Nursing, Medical Sciences, Life Sciences or related disciplines may be eligible. The vacancy provides multiple qualification pathways, including candidates with a Bachelor’s or Master’s degree, PharmD, Associate degree or relevant non-degree experience.
The application deadline listed for this position is October 12, 2026.
Fortrea Safety Science Coordinator II – Job Highlights
| Particular | Details |
|---|---|
| Company | Fortrea |
| Job Title | Safety Science Coordinator II |
| Location | Bangalore, India |
| Job Type | Full Time |
| Function | Clinical Safety / Pharmacovigilance |
| Experience | Varies by educational qualification |
| Eligible Fields | Pharmacy, Biological Sciences, Nursing, Medical Sciences, Life Sciences or related disciplines |
| Key Areas | Adverse Event Processing, Pharmacovigilance, MedDRA, Safety Reporting |
| Work Environment | Office or Remote |
| Requisition ID | 265159 |
| Application Deadline | October 12, 2026 |
| Salary / CTC | Not specified |
About Fortrea
Fortrea is a global clinical research organization that supports pharmaceutical, biotechnology and healthcare companies across clinical development and related research activities.
The Safety Science Coordinator II position supports clinical safety and pharmacovigilance operations, including the processing and reporting of safety information from clinical trials and post-marketing sources.
Job Description
The Safety Science Coordinator II will assist with Clinical Safety and Pharmacovigilance Safety Services (PSS) activities associated with pharmaceutical products.
The role involves receiving, processing, reviewing and reporting adverse event information according to client requirements, study plans and applicable regulatory timelines.
The professional will work with safety databases, regulatory reporting processes, medical reviewers, clients, investigators, regulatory authorities and other project stakeholders.
Safety Science Coordinator II – Role Overview
The position covers the complete handling of applicable safety cases, from initial receipt and data entry through medical review, coding, narrative preparation, quality checks and submission.
The role may support both clinical trial safety data and post-marketing adverse event reports, depending on the assigned project.
Educational Qualification
Fortrea provides multiple qualification pathways for this position.
Degree-Based Eligibility
Candidates may qualify with:
- BS/BA plus at least 1 year of relevant experience.
- MS/MA plus at least 1 year of relevant experience.
- PharmD plus at least 1 year of relevant experience.
For PharmD candidates, a one-year residency or fellowship may be considered relevant experience.
Other Qualification Pathways
The vacancy also indicates:
- Associate degree + 1 year of Safety experience, or 2 years of relevant experience.
- Non-degree qualification + 1 year of Safety experience, or 3 years of relevant experience.
Preferred Educational Disciplines
A degree or background in one or more of the following fields is preferred:
- Pharmacy
- Biological Sciences
- Nursing
- Medical Sciences
- Life Sciences
- Related scientific or healthcare disciplines
Experience Requirements
The required experience varies according to the candidate’s educational pathway.
Relevant experience may include work in:
- Pharmacovigilance
- Clinical Safety
- Adverse Event Processing
- Drug Safety
- Clinical Research
- Medical or Life Sciences
- Related safety operations
The vacancy also emphasizes accuracy, attention to detail, teamwork and the ability to work independently with moderate supervision.
Key Responsibilities
Adverse Event Processing
The selected candidate will:
- Process adverse event reports received from different sources according to client or sponsor plans.
- Handle safety cases originating from spontaneous reports.
- Process adverse events reported during clinical trials.
- Enter safety information into adverse event databases and tracking systems.
- Review cases for completeness, accuracy and suitability for expedited reporting.
- Ensure safety cases are processed according to applicable requirements and timelines.
Medical Review and Case Assessment
Responsibilities include:
- Identify clinically important information that may be missing from initial reports.
- Generate follow-up queries to obtain additional information.
- Consult medical staff when required.
- Ensure cases receive appropriate medical review.
- Assess cases for applicable reporting requirements.
- Ensure cases requiring expedited reporting receive appropriate priority.
MedDRA Coding and Patient Narratives
The role involves:
- Accurately coding adverse events using MedDRA, where applicable.
- Preparing patient narratives.
- Reviewing safety information for completeness and consistency.
- Performing appropriate label checks for marketed products when applicable.
Expedited Safety Reporting
The Safety Science Coordinator II will support expedited safety reporting activities, including:
- Processing cases requiring expedited reporting.
- Preparing and submitting expedited SAE reports.
- Supporting submissions to regulatory authorities.
- Coordinating submissions to Ethics Committees and investigators when required.
- Supporting reporting to clients, partners, vendors and Fortrea project personnel.
- Ensuring submissions are completed within applicable study or regulatory timelines.
Expedited and Periodic Safety Reports
The position also includes support for:
- Expedited Safety Reports (ESRs)
- Periodic Safety Reports (PSRs)
- Tracking of safety reporting activities
- Maintenance of reporting records
- Submission support for clients and relevant authorities
Documentation and Tracking
The selected candidate will:
- Maintain safety tracking systems.
- Set up and maintain project and central files.
- Maintain study-level and project-level documentation.
- Ensure required records are maintained according to project requirements.
- Support documentation associated with safety operations.
Quality Review and Reconciliation
Responsibilities may include:
- Supporting quality review of processed safety reports.
- Performing peer review activities when required.
- Assisting with database reconciliation.
- Supporting associated reconciliation activities.
- Ensuring the quality and accuracy of processed safety data.
Training and Team Support
The role may also involve:
- Supporting training activities for PSS staff.
- Mentoring team members when required.
- Providing peer support.
- Contributing to team knowledge and operational consistency.
Reporting and Metrics
The candidate may support:
- Monthly status reporting.
- Generation and maintenance of PSS metrics.
- Tracking operational activities.
- Preparation of information required for client reporting.
SOP and Regulatory Compliance
The position requires a strong understanding of:
- Standard Operating Procedures (SOPs)
- Work Instructions (WIs)
- Pharmacovigilance procedures
- Safety management guidance
- Safety reporting requirements
- Applicable regulatory directives
- Study and project plans
The candidate will be expected to ensure that safety operations comply with applicable requirements.
Client and Audit Support
The Safety Science Coordinator II may:
- Assist with preparation for client meetings.
- Liaise with client contacts when appropriate.
- Support quality issue management.
- Assist with audit preparation.
- Support inspection-readiness activities.
Additional responsibilities may be assigned by management based on project requirements.
Required Skills
Candidates should demonstrate:
- High accuracy and strong attention to detail.
- Good written communication skills.
- Good verbal communication skills.
- Ability to work effectively as part of a team.
- Ability to work independently with moderate supervision.
- Good organizational skills.
- Ability to handle safety information carefully and accurately.
- Knowledge of MS Office and Windows applications is beneficial.
- Good keyboard skills.
- Mentoring ability is preferred.
Pharmacovigilance Knowledge
Knowledge of safety operations is particularly relevant to this position. Candidates should be comfortable working with concepts such as:
- Adverse event reports
- Clinical trial safety
- Post-marketing safety
- SAE reporting
- Expedited reporting
- MedDRA coding
- Patient narratives
- Medical review
- Safety databases
- Pharmacovigilance SOPs
- Regulatory safety reporting
Work Location and Work Environment
- Location: Bangalore, India
- Job Type: Full Time
- Work Environment: Office or Remote
- Function: Clinical Safety / Pharmacovigilance
- Requisition ID: 265159
The vacancy specifically indicates that the position may be performed in an office environment or remotely.
Salary / CTC
Fortrea has not specified the salary or CTC for the Safety Science Coordinator II position in the available vacancy information.
Candidates should confirm compensation and other employment conditions during the official recruitment process.
Selection Process
The detailed selection process has not been specified in the vacancy information.
Candidates may be evaluated based on their educational qualification, relevant safety or clinical research experience, pharmacovigilance knowledge, communication skills, attention to detail and ability to handle safety data accurately.
How to Apply for Fortrea Safety Science Coordinator II
Interested and eligible candidates should apply through Fortrea’s official careers platform before the stated deadline.
Application Deadline
October 12, 2026
Candidates should review the complete vacancy requirements and submit their application before the closing date.
Important Details Before Applying
- The company is Fortrea.
- The position is Safety Science Coordinator II.
- The job location is Bangalore, India.
- This is a full-time position.
- The role supports Clinical Safety and Pharmacovigilance operations.
- Multiple educational and experience pathways are available.
- Relevant disciplines include Pharmacy, Biological Sciences, Nursing, Medical Sciences and Life Sciences.
- PharmD candidates with one-year residency or fellowship experience may be considered under the stated criteria.
- The role includes adverse event processing, MedDRA coding and safety reporting.
- Work may be performed in an office or remote environment.
- The requisition ID is 265159.
- The application deadline is October 12, 2026.
- Salary/CTC has not been disclosed.
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 position is based in Bangalore, India.
3. What type of work does this role involve?
The role focuses on Clinical Safety and Pharmacovigilance operations, particularly adverse event processing and safety reporting.
4. Is PharmD eligible for this position?
Yes. PharmD is one of the listed qualification pathways, with 1 year of relevant experience indicated. A one-year residency or fellowship may also be considered relevant experience.
5. Can Life Sciences graduates apply?
Yes. Life Sciences is one of the preferred educational disciplines listed for the position, subject to the applicable experience requirement.
6. What is MedDRA used for in this role?
MedDRA is used for the accurate coding of adverse events where applicable.
7. Does the job involve clinical trial safety data?
Yes. The role may involve processing adverse event information originating from clinical trials as well as post-marketing sources.
8. Does the position involve regulatory reporting?
Yes. The role includes supporting expedited safety reporting and submissions to regulatory authorities and other recipients when required.
9. Is remote work available?
The vacancy indicates an office environment or remote work arrangement.
10. What is the requisition ID?
The requisition ID is 265159.
11. What is the application deadline?
The listed deadline is October 12, 2026.
12. What is the salary for this position?
The salary or CTC has not been specified in the available vacancy information.
Important Note
Recruitment requirements, eligibility criteria, work arrangements, application deadlines and other employment conditions may change. Candidates should verify the latest vacancy information on Fortrea’s official careers platform before applying and should rely on the employer’s official communication for final recruitment terms.