PHARMAFull-time
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 Centralized Study Coordinator positions in its Clinical Operations team in Bangalore. Freshers and candidates with up to 5 years of experience are eligible to apply.
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
Clinical Study Coordination
CTMS
eTMF
EDC
IWRS
Trial Documentation
TMF Quality Control
ICH-GCP Guidelines
COMPENSATION & REWARDS
Salary: Competitive / Disclosed upon candidate shortlisting
Compensation is competitive and aligned with industry standard entry-level to mid-level salary benchmarks for study coordination roles in global 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
Joining Fortrea as a Centralized Study Coordinator offers entry-level and early-career professionals direct exposure to global clinical trials. Career progression opportunities include advancement into Senior Centralized Study Coordinator, Clinical Research Associate (CRA), or Clinical Project Management roles.
APPLICATION ADVISORY
Highlight education in Life Sciences/Pharmacy, familiarity with ICH-GCP principles, and any academic exposure or hands-on knowledge of clinical trial systems (CTMS, eTMF, EDC).
RECOMMENDED TRAINING
1/5
READY TO SUBMIT?
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