The Clinical Research Coordinator (CRC) supports the planning and execution of clinical studies under the supervision of the Principal Investigator (PI). This role is designed for Life Science Freshers to build a career in clinical study coordination, participant management, and regulatory compliance.
Key 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.
Education Qualification
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.
Required Skills
Basic knowledge of ICH-GCP Guidelines.
Strong clinical documentation and organizational skills.
Excellent communication and interpersonal abilities.
High attention to detail and time management.
Proficiency in MS Office (Word, Excel, Power Point).