Fortrea Hiring Sr. Study Coordinator
Fortrea Hiring Sr. Centralized Study Coordinator in Bengaluru: Clinical Research Professionals with 2–3 Years Experience
Fortrea is hiring for a Sr. Centralized Study Coordinator position based in Bengaluru, Karnataka, on a full-time basis. The role sits within Fortrea’s clinical operations function and is aimed at clinical research professionals with 2 to 3 years of hands-on experience, particularly those comfortable working across clinical trial systems, study databases, and investigator payment processes. For candidates actively searching for clinical research jobs in Bengaluru, this opening offers the chance to work with one of the world’s larger contract research organizations on real, ongoing clinical trial operations.
Company Overview
Fortrea is a global contract research organization (CRO) that partners with pharmaceutical, biotechnology, and medical device companies to manage clinical trials across Phase I through Phase IV, alongside clinical pharmacology and patient access solutions. Spun off as an independent, Nasdaq-listed company from Labcorp’s clinical development business in 2023, Fortrea carries forward decades of cumulative clinical research experience and now operates with a workforce of roughly 19,000 to 20,000 professionals supporting customers in more than 90 countries. The organisation positions itself around scientific rigor, agility, and a strong focus on accelerating the journey of new treatments from early-phase research to market, giving Bengaluru-based candidates exposure to a genuinely global clinical research environment rather than a purely regional operation.
Job Role & Responsibilities
The Sr. Centralized Study Coordinator role is structured around supporting study teams across several connected areas of clinical trial operations, in addition to other duties assigned by the study management team.
Clinical Systems & Database Management
The coordinator is responsible for managing clinical systems and access permissions, maintaining study databases such as CTMS, IWRS, and EDC, and supporting the study team with eTMF (electronic Trial Master File) management activities. This also includes setting up study systems for newly awarded studies and maintaining ongoing CTMS compliance.
Data Review & Study Support
A significant part of the role involves supporting data review activities, following up with CRAs to resolve outstanding issues or action items, and assisting study leads with data review tasks as needed. The coordinator also generates study-specific reports, manages project communications, and supports broader project teams with additional study-related activities.
Investigator Payment Processing
The role carries clear responsibility for investigator payment workflows, including reviewing EDC and contract details to mark line items as “Ready to Pay” or “Screen Failure” in CTMS, working with the Payment Administrator to generate cover letters or proforma invoices, and handling payment batch generation. The coordinator also performs invoice quality checks, prepares Good-Faith Invoice Approvals where applicable, coordinates line-item and GIA approvals with the Clinical Team Lead and Project Manager, processes out-of-pocket and pass-through expense invoices, and manages payment reconciliation during study close-out or on an ad hoc basis.
Documentation, Compliance & General Support
Beyond these core areas, the coordinator follows all applicable departmental SOPs and Work Instructions, completes required training within set timelines, and manages project and technical documentation appropriately. The role also includes assisting with document management up to eTMF filing, supporting new investigator submission packages for site or regulatory submission, helping study start-up teams with site activation tasks, and reviewing or supporting the management of site clinical trial contracts in line with defined processes and timelines.
Eligibility & Qualifications
Fortrea has laid out a clear set of minimum qualifications for this role:
- A university or college degree, with a Life Science background preferred, or a certification in an allied health profession from an accredited institution, such as a nursing certification, or medical or laboratory technology certification
- 2 to 3 years of work experience in clinical research, including a strong working knowledge of ICH-GCP guidelines and other applicable regulations and standards
- Fortrea may consider relevant and equivalent experience in place of the standard educational requirement
- Fluency in English, both written and verbal, along with demonstrated ability to organise work and communicate effectively, pay close attention to detail, and consistently deliver high-quality output while collaborating well with others
In terms of overall experience, candidates should have 2 to 3 years specifically within this job discipline, and may have between 0 to 3 years of experience in other professional roles prior to moving into clinical research.
Location & Salary
This role is based in Bengaluru, Karnataka, one of India’s key hubs for clinical research and life sciences operations. Fortrea has not disclosed a specific salary figure for this opening. Based on prevailing compensation trends for Senior Study Coordinator and similar clinical trial support roles with 2 to 3 years of experience at global CROs in India, candidates can expect an estimated annual package in the range of ₹6 LPA to ₹10 LPA, depending on prior experience, system exposure, and qualifications.
Application Process
Candidates can apply directly through Fortrea’s official Workday careers portal for this requisition.
Apply for Sr. Centralized Study Coordinator – Bengaluru
Frequently Asked Questions
How much experience is required for this role? Fortrea requires 2 to 3 years of work experience in clinical research, along with a strong working knowledge of ICH-GCP guidelines.
What educational background is needed? A university or college degree, preferably in Life Sciences, or an allied health certification such as nursing, medical, or laboratory technology, is required. Fortrea may also consider equivalent relevant experience in place of formal education.
Where is this job located? The role is based in Bengaluru, Karnataka, India.
What is the expected salary for this position? Fortrea has not disclosed an exact figure. Based on industry trends for similar roles, the estimated range is approximately ₹6 LPA to ₹10 LPA.
How do I apply for this position? You can apply directly through Fortrea’s official Workday careers portal using the link provided in this posting.
| Company | Fortrea |
| Vacancies | Sr. Centralized Study Coordinator |
| Required Education | University/College Degree (Life Science preferred), Nursing Certification, Medical or Laboratory Technology Certification |
| Experience | 2–3 Years in Clinical Research |
To apply for this job please visit fortrea.wd1.myworkdayjobs.com.
