Clinical Research Coordinator - Freshers

About the Role

The Clinical Research Coordinator (CRC) supports the planning and execution of clinical studies under the supervision of the Principal Investigator (PI).

Responsibilities

• Study Coordination: Assist in managing clinical research as per approved protocols.
• Participant Management: Schedule visits and maintain accurate subject records.
• Screening: Evaluate potential participants based on study eligibility criteria.
• Informed Consent: Support the consent process and explain procedures to subjects.
• Data Management: Record trial data in Case Report Forms (CRFs) and electronic systems.
• Regulatory Filing: Maintain study files and essential regulatory documents.
• GCP Compliance: Ensure all trial activities follow Good Clinical Practice guidelines.
• Audit Support: Assist the team during monitoring visits and site audits.

What You'll Need

• B.Sc / M.Sc in Life Sciences (Microbiology, Biotechnology, Nursing).
• B.Pharm / M.Pharm / D.Pharm.
• BDS / BHMS / BAMS.
• Degrees in Clinical Research or Allied Health Sciences.

Resume Tip

Highlight your basic knowledge of ICH-GCP Guidelines, strong clinical documentation and organizational skills, excellent communication and interpersonal abilities, high attention to detail and time management, and proficiency in MS Office (Word, Excel, PowerPoint).