Clinical Trial Coordinator (Fresher)
Actively Reviewing the ApplicationsClinoGenesis Research Institute
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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