Fortrea Careers is hiring for two exciting clinical research positions in Bangalore โ TMF Classifier I and Central Monitor Assistant. These opportunities are ideal for candidates with Life Sciences backgrounds looking to build careers in clinical operations, eTMF management, study support, and clinical data review.
Candidates with experience in clinical research, eTMF, CTMS, GCP, ICH guidelines, and regulatory documentation are encouraged to apply. Both roles offer strong exposure to global clinical trials and sponsor-facing operations.
Fortrea Recruitment 2026 Overview
| Company | Fortrea |
|---|---|
| Job Roles | TMF Classifier I, Central Monitor Assistant |
| Location | Bangalore |
| Job Type | Full-Time |
| Mode | Hybrid (TMF Classifier I) |
| Qualification | B.Sc, B.Pharm, M.Pharm, Life Sciences, Nursing, Biotechnology |
| Experience | 0 โ 3 Years |
| Industry | Clinical Research / CRO |
| Last Date | May 18, 2026 (TMF Classifier I) |
TMF Classifier I at Fortrea
The TMF Classifier I role focuses on managing electronic Trial Master Files (eTMF), audit readiness, Smart Inbox classification, ARC review, and regulatory document quality checks.
Key Responsibilities
- Manage eTMF documentation for clinical studies
- Perform Smart Inbox classification and ARC review
- Conduct audit-ready checks on uploaded study documents
- Maintain compliance with ICH-GCP and regulatory requirements
- Support sponsor audits and internal QA audits
- Track essential trial artifacts throughout study phases
- Collaborate with study teams and startup teams
- Ensure document readability and image clarity before release
- Handle operational issues related to TMF management
Eligibility Criteria
- Bachelorโs Degree in Life Sciences or Business-related field
- 6โ12 months of experience in clinical research environment
- Understanding of GCP and ICH guidelines
- Knowledge of regulatory and clinical documentation
- Familiarity with Microsoft Office and Adobe Acrobat
Preferred Qualifications
- Masterโs Degree in Life Sciences/Business
- Experience working with clinical electronic systems
- Strong communication and interpersonal skills
Central Monitor Assistant at Fortrea
The Central Monitor Assistant role involves clinical systems support, CTMS management, study reporting, investigator payment support, and clinical trial documentation activities.
Key Responsibilities
- Manage study databases including CTMS, IWRS, and EDC
- Support eTMF management and study documentation
- Generate study reports and maintain project communications
- Perform access management for clinical systems
- Assist in investigator payment processing and reconciliation
- Support startup teams and regulatory submission activities
- Follow up on study queries and data review tasks
- Assist in site startup and contract management activities
Eligibility Criteria
- Degree in Life Sciences, Nursing, Medical Laboratory Technology, or related fields
- 2โ3 years of clinical research experience
- Strong knowledge of ICH-GCP guidelines
- Good communication and organizational skills
- Ability to manage multiple study support activities
Why Join Fortrea?
Fortrea Official Website is one of the leading global Contract Research Organizations (CROs), offering excellent career growth opportunities in clinical operations, pharmacovigilance, clinical data management, TMF management, and regulatory support.
Employee Benefits
- Global clinical trial exposure
- Hybrid work opportunities
- Career advancement in clinical research
- International project collaboration
- Learning and certification support
- Competitive salary packages
Salary Details
Based on industry standards in Bangalore clinical research market:
| Role | Estimated Salary |
|---|---|
| TMF Classifier I | โน3.5 โ โน5.5 LPA |
| Central Monitor Assistant | โน5 โ โน8 LPA |
How to Apply for Fortrea Jobs?
Interested and eligible candidates can apply directly through the official Fortrea careers portal:
Apply for Central Monitor Assistant
