Fortrea has announced Clinical Data Management jobs in Bangalore for professionals interested in clinical research and data management. The company is recruiting for two positions: Clinical Data Analyst โ CPS Data Management and Senior Clinical Data Analyst.
These Fortrea Clinical Data Analyst jobs involve clinical trial data review, query management, data reconciliation, edit check testing, database activities and clinical data management documentation. Candidates with educational backgrounds in life sciences, health sciences, information technology or allied health professions may be eligible.
The Clinical Data Analyst position requires approximately 1โ2 years of clinical research experience, while the Senior Clinical Data Analyst position requires 2โ4 years of applicable clinical research experience, preferably within clinical data management.
Fortrea Hiring 2026 โ Job Overview
| Particular | Details |
|---|---|
| Company | Fortrea |
| Role 1 | Clinical Data Analyst โ CPS Data Management |
| Role 2 | Senior Clinical Data Analyst |
| Department | CPS Data Management / Clinical Data Management |
| Location | Bangalore, Karnataka |
| Employment | Full-Time |
| Qualification | Life Sciences / Health Sciences / IT / Allied Health or related |
| Experience โ Role 1 | 1โ2 Years |
| Experience โ Role 2 | 2โ4 Years |
| Application Deadline | September 2, 2026 |
Role 1: Clinical Data Analyst โ CPS Data Management
The Clinical Data Analyst โ CPS Data Management will perform clinical data management activities supporting the Lead Data Reviewer or Lead Data Manager. The position focuses on ensuring clinical trial data meets project timelines, productivity expectations and client quality requirements.
Key Responsibilities
- Perform clinical trial data review and query management activities.
- Review data according to Data Management Plans, Edit Check Specifications and Data Review Guidelines.
- Identify erroneous, incomplete or missing clinical data.
- Generate, resolve and track clinical data queries.
- Perform reconciliation activities.
- Generate diagnostics, special listings and reconciliation discrepancy listings.
- Support clinical database setup, maintenance and project closure activities.
- Assist in creating and reviewing Edit Check Specifications.
- Create dummy data for testing database edit checks.
- Test database screens and functionality.
- Assist with dummy data testing for SAS reports and data listings.
- Maintain Data Management documentation.
- Support maintenance of relevant eTMF documentation.
- Generate assigned clinical study status reports.
- Coordinate with other clinical project team members.
- Perform additional data management responsibilities as assigned.
Qualification
Candidates should have a university or college degree in life sciences, health sciences, information technology or a related discipline, or certification in an appropriate allied health profession.
Relevant educational backgrounds may include degrees such as B.Pharm, M.Pharm, Pharm.D, B.Sc/M.Sc Life Sciences, Biotechnology, Microbiology, Biochemistry, Clinical Research, Nursing, Health Sciences, B.Tech Biotechnology, BCA, B.Sc IT, B.Tech IT/Computer Science or other relevant qualifications, subject to Fortrea’s assessment of the candidate’s education against the official eligibility criteria.
Experience Required
Applicants should have approximately 1โ2 years of clinical research experience.
Candidates should also demonstrate:
- Good written and verbal communication skills.
- Strong interpersonal abilities.
- Ability to collaborate effectively in a team environment.
- Good organizational skills.
- Ability to work with project teams and clinical data.
Fortrea also states that additional relevant experience may be considered in place of certain education requirements.
Role 2: Senior Clinical Data Analyst
The Senior Clinical Data Analyst will have greater responsibility for coordinating clinical data review, query generation and resolution, reconciliation and other Clinical Data Management activities.
The selected candidate will support the Data Management Lead and may serve as a backup to the Clinical Data Manager for assigned clinical data management activities.
Key Responsibilities
- Coordinate clinical data review and query management activities.
- Ensure assigned projects follow protocols, applicable SOPs and GCP requirements.
- Review clinical trial data according to Data Management Plans and study specifications.
- Generate, resolve and track clinical data queries.
- Perform aggregate clinical data review.
- Execute programs, special listings and reconciliation discrepancy listings.
- Review data listings for internal data review.
- Create dummy data for edit-check testing and database functionality testing.
- Support testing of SAS reports and clinical data listings.
- Modify templates to develop study-specific Data Management Plans.
- Support preparation of eCRF completion guidelines.
- Maintain Data Management documentation and relevant eTMF records.
- Generate clinical study status reports.
- Perform database extracts.
- Support preparation of Investigator Meeting and Site Initiation Visit materials.
- Assist with Database Lock activities.
- Support training of new employees on project-specific Clinical Data Management processes.
- Work with cross-functional clinical project teams throughout study setup, maintenance and closure.
Senior Clinical Data Analyst Qualification
Candidates should possess a university/college degree in life sciences, health sciences, information technology or a related discipline, or an appropriate allied health professional certification.
Applicants should also be fluent in written and spoken English.
Experience Required
The Senior Clinical Data Analyst position requires approximately 2โ4 years of applicable clinical research experience, with Clinical Data Management experience preferred.
Candidates should have knowledge or understanding of:
- Clinical Data Management practices
- Medical terminology
- Drug development process
- Clinical trial data review
- Query management
- Data reconciliation
- Database activities
- GCP requirements
- Project timelines and productivity metrics
Strong communication, organization, teamwork and time-management skills are also expected.
Who Can Apply?
Candidates from relevant Life Sciences, Pharmacy, Health Sciences, Clinical Research, Biotechnology, Nursing and Information Technology backgrounds can review their eligibility for these Fortrea Clinical Data Analyst openings.
Qualification in short: Life Sciences / Health Sciences / IT / Allied Health-related degree or certification.
Skills Relevant to Fortrea Clinical Data Analyst Jobs
Professionals applying for these Clinical Data Management jobs in Bangalore can benefit from experience or knowledge in:
- Clinical Data Management (CDM)
- Clinical trial data review
- Query generation and resolution
- Data reconciliation
- Edit checks
- eCRF/CRF review
- Database testing
- Data Management Plans
- eTMF documentation
- Medical terminology
- GCP
- Drug development
- Database lock activities
- SAS reports/data listings
Salary
For informational purposes only, comparable Clinical Data Analyst and Senior Clinical Data Analyst positions in India’s CRO and clinical research sector can vary substantially according to experience, CDM expertise, employer compensation structure and responsibilities. Applicants should therefore confirm the actual compensation directly with Fortrea during the recruitment process rather than treating third-party salary estimates as the offered salary.
Benefits and Work Environment
The supplied job description indicates an office and/or home-based work environment. Other compensation, insurance, leave, incentives or employee benefits were not specified in the provided vacancy information and should be confirmed during the recruitment process.
Potential career exposure from these positions includes hands-on work with clinical trial data review, database processes, query management, reconciliation, clinical documentation and cross-functional clinical research teams.
How to Apply
