Fortrea, a leading global clinical research organization (CRO), is hiring for the position of Central Monitor Assistant in Bangalore, India. This is an excellent opportunity for professionals with experience in clinical research, clinical trial management, eTMF management, CTMS, investigator payments, and study support activities.
Candidates with a Life Sciences background and 2–3 years of clinical research experience can apply for this exciting Fortrea career opportunity. If you are looking for a clinical operations job in Bangalore, this opening offers exposure to global clinical trials, study management, data review, and investigator payment processing.
Job Details
| Particulars | Details |
|---|---|
| Position | Central Monitor Assistant |
| Company | Fortrea |
| Location | Bangalore, Karnataka, India |
| Employment Type | Full-Time |
| Experience | 2–3 Years |
| Qualification | Life Sciences Degree Preferred |
| Application Deadline | June 30, 2026 |
About Fortrea
Fortrea is a globally recognized Contract Research Organization (CRO) dedicated to advancing life-saving therapies through innovative clinical development solutions. The company supports pharmaceutical, biotechnology, and medical device organizations worldwide through clinical trial management, patient-focused research, and regulatory support services.
Key Responsibilities
The selected candidate will be responsible for:
Clinical Trial Support
- Manage clinical systems and user access management.
- Maintain study databases including CTMS, IWRS, and EDC systems.
- Support study teams in eTMF management activities.
- Assist with clinical data review and study support functions.
- Generate study-specific reports and documentation.
Data Review Activities
- Follow up with Clinical Research Associates (CRAs) regarding outstanding issues.
- Support lead monitors in study-specific data review tasks.
- Ensure timely resolution of data discrepancies.
Study Operations Support
- Perform study system setup for newly awarded studies.
- Support CTMS compliance management.
- Manage project communications and coordination.
- Assist startup and study teams with operational activities.
Investigator Payment Processing
- Review EDC and contract information.
- Process investigator payments and payment reconciliations.
- Prepare payment documentation and quality control checks.
- Coordinate approvals with project teams.
- Process pass-through expenses and out-of-pocket invoices.
Documentation & Compliance
- Maintain project documentation and study records.
- Support investigator submission package preparation.
- Manage document collection, review, tracking, and eTMF filing.
- Follow applicable SOPs, work instructions, and ICH-GCP requirements.
Required Qualifications
Candidates should possess:
- University degree in Life Sciences, Pharmacy, Biotechnology, Clinical Research, Nursing, Medical Laboratory Technology, or related healthcare discipline.
- Strong understanding of ICH-GCP guidelines.
- Excellent written and verbal English communication skills.
- Strong organizational and documentation skills.
- High attention to detail and quality standards.
- Ability to work collaboratively in cross-functional teams.
Experience Requirements
- They prefer candidates who have 2–3 years of relevant clinical research experience (CTMS, eTMF, study support, clinical operations, investigator payments, etc.).
- However, they may also consider candidates who have 0–3 years of experience in related roles if their skills match the job requirements.
- Experience with CTMS, EDC, IWRS, eTMF, or related clinical systems.
- Knowledge of clinical operations and investigator payment processes is preferred.
- Experience supporting clinical trials and study management activities.
Why Join Fortrea?
Benefits of Working at Fortrea
- Opportunity to work with a leading global CRO.
- Exposure to international clinical trials.
- Career growth in clinical operations and study management.
- Collaborative and innovative work environment.
- Training and professional development opportunities.
- Experience working on life-changing therapies and patient-focused research.
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How to Apply
