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Clinical Research Coordinator (Crc) Intern

AGenome Research
Fresher years
5k - 8k
Pune, India
10 June 1, 2026
Job Description
Job Type: Full Time Education: M.Pharm/B.Pharm or M.Sc. Skills: ICSR Case Processing, Interpersonal Skill, Labelling Assessment

Clinical Research Coordinator (CRC) Intern

Location: Pune (Alandi, Katraj, Kothrud), Latur, Ahilyanagar
Company: AGenome Research
Experience Level: Freshers Only
Open Positions: 10
Qualification: B.Sc Biotechnology / B.Pharm / M.Pharm (Passed-Out Candidates Only)

Job Overview

The Clinical Research Coordinator (CRC) Intern will support the execution and coordination of clinical research studies at investigational sites. The role involves assisting investigators, managing study documentation, coordinating participant visits, and ensuring compliance with clinical research regulations and protocols.

This internship provides hands-on exposure to clinical trial operations, patient coordination, regulatory documentation, and site management activities, making it an excellent opportunity for candidates seeking a career in Clinical Research.

Key Responsibilities

A. Clinical Trial Coordination

Support day-to-day clinical trial activities at assigned research sites.
Assist investigators and site staff in conducting study-related procedures.
Coordinate participant visits, appointments, and follow-up activities.
Maintain study schedules and ensure timely completion of site activities.
Support subject recruitment and retention activities as per study requirements.

B. Patient & Site Management

Coordinate communication between study participants and investigators.
Assist in screening and enrollment activities.
Ensure proper documentation of participant visits and study procedures.
Maintain participant confidentiality and data privacy standards.
Support collection and management of informed consent documentation.

C. Regulatory & Documentation Support

Maintain Investigator Site Files (ISF) and study-related documentation.
Assist in preparing essential documents for study initiation and ongoing site activities.
Ensure documentation is complete, accurate, and audit-ready.
Support filing and tracking of regulatory and ethics committee documents.

D. Data Collection & Quality Management

Assist in source documentation and case report form completion.
Support data entry, verification, and quality review activities.
Identify and report documentation discrepancies to site coordinators.
Ensure data accuracy and compliance with study protocols.

Interested candidates may send their updated CV to:

career@agenomeresearch.com

Subject Line Format:
(Location) – (Qualification) – CRC Intern