Life Sciences Jobs at Fortrea in Bengaluru | Apply Online
Looking for exciting Life Sciences Jobs with a leading global CRO? Fortrea is hiring a Central Monitor Assistant in Bangalore, offering an excellent opportunity for professionals seeking growth in Clinical Research Jobs and study management operations. This role provides exposure to clinical trial systems, investigator payments, eTMF management, CTMS compliance, and study support activities. If you are planning to build a long-term Fortrea Career, this position can help you gain valuable experience within a globally recognized clinical research organization.
- Job Title: Central Monitor Assistant
- Location: Bangalore
- Employment Type: Full time
- Job Requisition ID: 262504
About the Company
Fortrea is a leading global contract research organization (CRO) dedicated to advancing life-saving therapies for patients worldwide. The company supports pharmaceutical, biotechnology, and healthcare organizations through comprehensive clinical development solutions, data management services, and clinical operations expertise. With a strong focus on innovation, quality, and collaboration, Fortrea provides professionals with opportunities to contribute to clinical trials and healthcare advancements while developing rewarding careers in clinical research.
Key Responsibilities
- Manage clinical systems and access management
- Maintain study databases (CTMS, IWRS, EDC, etc.)
- Support e-TMF management and document tracking
- Conduct data review and follow up on action items
- Generate study-specific reports
- Perform study system setup for new awarded studies
- Manage investigator payment processing and reconciliation
- Ensure compliance with departmental SOPs and required trainings
Eligibility Criteria
Education: University/College Degree (Life Science preferred), or certification in an allied health profession from an accredited institution (e.g., Nursing certification, Medical or laboratory technology).
Experience: 02-03 years of work experience in clinical research with strong knowledge of ICH-GCP guidelines and applicable regulations.
Required Skills
- Strong understanding of ICH-GCP and regulatory guidelines
- Clinical systems management (CTMS, IWRS, EDC)
- Data review and issue resolution
- Documentation and e-TMF handling
- Attention to detail and quality checks
- Project communication and coordination
- Ability to work collaboratively
- Proficiency in computer and departmental tools
- Fluent in English, both written and verbal.
For professionals seeking Life Sciences Jobs, this opening offers a valuable opportunity to gain hands-on experience in clinical trial operations, study management, and regulatory support. Through a rewarding Fortrea Career, candidates can strengthen their expertise in global clinical development processes while contributing to meaningful healthcare advancements. Those interested in Clinical Research Jobs should consider applying before the application deadline.
