PHARMAFull-time
Senior Centralized Study Coordinator
BANGALORE (IN)ONSITEPOSTED: 8/7/2026
PHARMAFull-time
HIRING ORGANIZATIONFORTREAContract Research Organization (CRO) / Biosciences / Healthcare
ROLE DEFINITION & RESPONSIBILITIES
Global Clinical Research Organization (CRO) Fortrea has opened applications for Senior Centralized Study Coordinator positions in its Clinical Operations team in Bangalore.
Key Responsibilities
Managing clinical systems and user access management.
Maintaining study documentation at study, country, and site levels.
Updating CTMS, IWRS, EDC, and other clinical databases.
Supporting electronic Trial Master File (eTMF) management.
Performing TMF quality control and archival activities.
Tracking study milestones, timelines, and project metrics.
Preparing CRA Prep Packs before monitoring visits.
Coordinating with CRAs to resolve outstanding site issues.
Supporting clinical data review activities.
Updating XRIM and project governance tools.
Tracking protocol deviations and action items.
Coordinating meetings and documenting meeting minutes.
Supporting vendor management activities.
Managing invoice trackers and purchase order requests.
Maintaining project documentation and compliance metrics.
Supporting project plans and study execution.
Participating in process improvements and SOP compliance.
Assisting study teams with cross-functional operational activities.
Qualifications
B.Pharm, M.Pharm, Pharm.D, B.Sc/M.Sc Life Sciences, Biotechnology, Clinical Research, Nursing, Biomedical Sciences, or related healthcare/life science degree.
REQUIRED VERIFIED SKILLS
Clinical Operations
Centralized Study Coordination
CTMS
eTMF
EDC
IWRS
TMF Quality Control
Protocol Deviation Tracking
ICH-GCP Guidelines
COMPENSATION & REWARDS
Salary: Competitive / Disclosed upon candidate shortlisting
Salary is based on market rates for experienced study coordinators in top-tier Contract Research Organizations (CROs).
ORGANIZATION CONTEXT & CULTURE
Fortrea is a global contract research organization (CRO) providing comprehensive clinical development, patient access, and laboratory services. Spun off from Labcorp in 2023, Fortrea partners with pharmaceutical, biotech, and medical device companies to accelerate the development and commercialization of new therapies. They offer a full suite of services across the entire drug development lifecycle.
TEAM SIZE: 19,000+ employees
INDUSTRY: Contract Research Organization (CRO) / Biosciences / Healthcare
EXPECTED CAREER ROADMAP
This senior role provides pathway opportunities toward Lead Study Coordinator, Clinical Trial Manager, and regional Clinical Operations leadership positions within Fortrea's multinational network.
APPLICATION ADVISORY
Emphasize previous experience with TMF quality audits, complex CTMS management, protocol deviation tracking, and cross-functional team coordination during global clinical trials.
RECOMMENDED TRAINING
1/5
READY TO SUBMIT?
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