Clinical Research Coordinator (CRC) - Freshers Only

About the Role

We are seeking a detail-oriented and motivated Clinical Research Coordinator (CRC) to support the successful execution of clinical trials in accordance with ICH-GCP, study protocols, and regulatory guidelines.

Responsibilities

• Coordinate and manage clinical trial activities from study initiation to close-out.
• Screen, recruit, and schedule eligible study participants.
• Obtain and document informed consent according to study protocols.
• Coordinate study visits and follow-up appointments.
• Collect, verify, and maintain accurate clinical research data and source documents.
• Ensure compliance with ICH-GCP, SOPs, protocol requirements, and regulatory guidelines.
• Maintain Investigator Site Files (ISF), Trial Master Files (TMF), and essential study documents.
• Report adverse events (AEs) and serious adverse events (SAEs) as per protocol.
• Coordinate with Principal Investigators, sponsors, CROs, monitors, and ethics committees.
• Prepare for monitoring visits, audits, and regulatory inspections.
• Maintain study records, logs, and documentation with high accuracy.

What You'll Need

• Bachelor's or Master's degree in Life Sciences, Pharmacy, Nursing, Biotechnology, Biochemistry, Microbiology, Clinical Research, or related disciplines.
• Knowledge of ICH-GCP, clinical trial processes, and regulatory requirements.
• Good documentation and organizational skills.
• Excellent communication and interpersonal skills.
• Proficiency in Microsoft Office (Word, Excel, PowerPoint).

Resume Tip

Highlight your knowledge of ICH-GCP, clinical trial processes, and regulatory requirements, as well as your experience with clinical documentation and source data verification.