Clinical Trial Coordinator

2 days ago

Bangalore, India ClinoGenesis Research Institute Full time

Job Description – Clinical Trial Coordinator (CTC) | Hyderabad About the Role The Clinical Trial Coordinator (CTC) plays a key role in supporting the planning, initiation, execution, and close-out of clinical trials. This role involves coordinating between investigators, clinical research staff, sponsors, and ethics committees to ensure smooth trial operations and compliance with regulatory and ethical guidelines. Key Responsibilities 1️⃣ Study Coordination & Site Management Assist in setting up and initiating clinical trials at the site Ensure all study supplies, documents, and equipment are available Maintain Investigator Site File (ISF) and Essential Documents Coordinate participant recruitment, screening, informed consent, and follow-up Support investigators in scheduling study visits and managing study calendars 2️⃣ Data Management & Documentation Perform accurate and timely data entry in EDC/eCRF systems Review source documents and ensure data accuracy & query resolution Maintain study logs: screening, enrollment, adverse events, delegations, etc. Assist in preparing regulatory documents and submissions for IEC/IRB 3️⃣ Regulatory & Compliance Support Ensure trial conduct complies with ICH-GCP, SOPs, and protocol requirements Assist with SAE reporting, protocol deviations, and adherence monitoring Prepare for site audits/monitoring visits and support response to findings 4️⃣ Participant Coordination Manage patient flow for study visits and ensure protocol-specified procedures Educate participants about study requirements and follow-up schedules Assist in sample collection, processing, and shipment as per guidelines 5️⃣ Stakeholder Collaboration Work closely with CRAs, sponsors, investigators, and hospital departments Support communication and coordination between clinical and research teams Required Qualifications & Skills Education B.Pharm / M.Pharm / B.Sc / M.Sc (Life Sciences, Biotechnology, Nursing, or related field) Experience 0–3 years of experience in clinical research, site coordination, or related domain Freshers with strong interest in clinical research may also be considered (optional based on employer) Technical Skills Knowledge of ICH-GCP guidelines Familiarity with eCRF/EDC systems Understanding of regulatory documentation Knowledge of clinical trial phases and site workflows Soft Skills Excellent communication & interpersonal skills Strong organizational and multitasking ability Attention to detail and documentation accuracy Ability to work in a hospital/clinical research environment What the Role Offers Hands-on experience in clinical trial operations Exposure to regulatory and ethical processes Collaboration with experienced investigators and CRAs Career growth in clinical research, site management, & pharmacovigilance

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