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Clinical Trial Coordinator (Fresher)

Actively Reviewing the Applications

ClinoGenesis Research Institute

India, Karnataka, Bengaluru Full-Time On-site
Posted 1 day ago Apply by June 1, 2026

Job Description

Clinical Research Coordinator (Fresher)


Location: Remote

Department: Clinical Research

Employment Type: Full-Time


Job Summary:


We are looking for a highly motivated and detail-oriented Clinical Research Coordinator (Fresher) to support the execution of clinical trials in compliance with ICH-GCP guidelines, regulatory requirements, and study protocols. The candidate will assist in coordinating clinical research activities, maintaining documentation, and ensuring subject safety and data integrity.


Key Responsibilities:


Assist in the coordination and management of clinical trials (Phase I–IV studies)


Ensure compliance with ICH-GCP, FDA, DCGI, and regulatory guidelines


Support in site initiation, monitoring, and close-out visits


Maintain and update Trial Master File (TMF) and Investigator Site File (ISF)


Assist in informed consent process (ICF) documentation


Coordinate with Principal Investigator (PI), Sub-Investigators, Sponsors, and CROs


Ensure accurate data entry in Case Report Forms (CRF/eCRF)


Handle source documentation and query resolution


Track and report Adverse Events (AE) and Serious Adverse Events (SAE)


Maintain subject recruitment and retention records


Schedule patient visits and follow-up appointments


Support in regulatory submissions and ethics committee documentation


Eligibility Criteria:


Bachelor’s or Master’s degree in Life Sciences, Pharmacy, Nursing, Biotechnology, Microbiology, or related field


Freshers or candidates with internship in Clinical Research / Clinical Trials


Knowledge of GCP, Clinical Trial Process, Regulatory Guidelines


Strong documentation and communication skills


Basic understanding of Medical Terminology and Pharmacovigilance


Required Skills:


Clinical Research, Clinical Trials, GCP, ICH Guidelines, FDA Regulations, DCGI, TMF, ISF, CRF, eCRF, AE/SAE Reporting, Regulatory Documentation, Ethics Committee, Site Management, Data Management, Monitoring Support, Pharmacovigilance, CRO, Investigator Coordination, Source Documentation, Patient Recruitment.

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