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Fortrea
Fortrea is inviting applications for the position of Central Monitor Assistant at its Bengaluru, Karnataka location. This is an excellent opportunity for professionals with 2–3 years of experience in clinical research who are looking to build a career with a leading global contract research organization (CRO).
About Fortrea
Fortrea is a leading global clinical research organization dedicated to transforming drug and device development. The company supports pharmaceutical, biotechnology, and medical device organizations worldwide through innovative clinical trial solutions and scientific expertise.
Job Details
| Particulars | Details |
|---|---|
| Position | Central Monitor Assistant |
| Location | Bengaluru, Karnataka, India |
| Experience | 2–3 Years |
| Qualification | University/College Degree (Life Science Preferred) |
| Industry | Clinical Research / CRO |
| Employment Type | Full-Time |
Key Responsibilities
Clinical Systems & Study Management
- Manage clinical systems and access management.
- Maintain study databases including CTMS, IWRS, EDC, and related systems.
- Support study teams in eTMF management activities.
- Assist in study data review and support activities.
- Generate study-specific reports.
- Perform study system setup for newly awarded studies.
- Ensure CTMS compliance management.
Data Review Activities
- Follow up with CRAs regarding resolution of outstanding issues and action items.
- Assist study leads with study-specific data review tasks.
- Support data quality and compliance initiatives.
Study Support Functions
- Generate study reports and project communications.
- Support site startup activities.
- Assist project teams with various study-related tasks.
- Manage technical and project documentation.
- Track, review, and report study metrics.
Investigator Payment Processing
- Review EDC and contracts and mark payment-related line items in CTMS.
- Generate payment batches and invoices.
- Perform invoice quality checks and reconciliation activities.
- Process out-of-pocket and pass-through expense invoices.
- Coordinate with study teams for approvals and payment processing.
Regulatory & Documentation Support
- Assist in document management and eTMF filing.
- Support investigator submission package preparation.
- Manage site clinical trial contracts.
- Create and manage iSite Packs.
- Ensure adherence to SOPs, work instructions, and quality standards.
Eligibility Criteria
Educational Qualification
- Bachelor’s or Master’s degree in Life Sciences preferred.
- Nursing, Medical Technology, Laboratory Technology, or allied healthcare certifications may also be considered.
- Equivalent relevant experience may be considered in lieu of educational requirements.
Experience Required
- 2–3 years of experience in clinical research.
- Strong understanding of ICH-GCP guidelines and applicable regulations.
- Experience with clinical trial systems and documentation processes preferred.
Required Skills
- Strong organizational and communication skills.
- Excellent attention to detail.
- Ability to work collaboratively in a team environment.
- High-quality work delivery and productivity focus.
- Proficiency in computer applications and clinical research tools.
- Strong documentation and reporting abilities.
- Fluent English communication skills (written and verbal).
Why Join Fortrea?
- Opportunity to work with a globally recognized CRO.
- Exposure to international clinical research projects.
- Career growth in clinical operations and study management.
- Collaborative and professional work environment.
- Hands-on experience with advanced clinical trial systems and processes.
How to Apply
Interested and eligible candidates can apply through the official Fortrea careers portal and search for the Central Monitor Assistant position in Bengaluru.
To apply for this job please visit fortrea.wd1.myworkdayjobs.com.
