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Chellaram Hospital
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Clinical Research Coordinator

Clinical Research Coordinator

Chellaram Hospital

2 - 6 years

4 - 8 Lacs

pune

Posted:1 day ago| Platform:

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Skills Required

site management gcp edc clinical trials clinical research life sciences ms office monitoring clinical data recruitment

Work Mode

Work from Office

Job Type

Full Time

Job Description

Knowledge of guidelines and regulatory requirements
Familiarity with clinical trial protocols and documentation
Excellent organizational and interpersonal communication skills
Proficiency in MS Office, EDC systems, and medical terminology

Job Responsibilities: Study Coordination:

Coordinate and manage day-to-day activities for clinical trials
Ensure proper patient recruitment, screening, informed consent, and enrollment
Schedule and manage study visits and procedures per protocol

Regulatory & Ethics Compliance:

Prepare, submit, and maintain documents for Institutional Ethics Committee (IEC) and sponsor approvals
Ensure adherence to ICH-GCP, protocol requirements, and SOPs
Maintain essential trial documents in the investigator site file (ISF)

Data & Documentation:

Accurately collect and enter clinical data into CRFs/EDCs
Assist in adverse event (AE/SAE) reporting and follow-up
Ensure timely query resolution and data clarification

Site Management:

Act as a point of contact between investigators, subjects, sponsors, and monitors
Support during site initiation, monitoring, and close-out visits
Participate in audits and inspections and ensure readiness

Patient Engagement:

Educate and support participants throughout the study
Maintain confidentiality and ethical standards in patient interactions

Working Conditions:

Hospital/research site-based role
May involve flexible working hours based on study requirements
Occasional travel for multi-site coordination (if applicable)

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