Headline

Clinical Research Trainee | ICH-GCP Certified | Clinical Documentation • EDC • Query Management | Seeking Entry-Level CRO Opportunities

About

I am a detail-oriented Clinical Research Professional currently gaining hands-on experience in Phase II–III clinical trials. I support patient screening, informed consent, source documentation, SDV, and data entry while ensuring strict adherence to GCP and study protocols. My experience includes query resolution, ISF maintenance, audit-ready documentation, and routine site operations. I collaborate closely with investigators, study coordinators, nurses, and monitors to ensure smooth and compliant trial conduct. I am passionate about clinical operations and data quality and aim to grow as a CRC/CTA/Clinical Data Professional.

Location

Kochi

Work experience

Training Specialist at Beaks Molecular Research Laboratory, Dec 2024 - Present · 1 yr 7 mos, Conducted a 1-month research project focused on identifying fish species through DNA barcoding techniques. Extracted and analyzed DNA samples, amplified target regions using PCR, and compared sequences for species verification. Gained hands-on experience with molecular biology techniques and data interpretation.

Trainee at Amrita Institute of Medical Sciences and Research Centre, Oct 2025 - Jan 2026 · 4 mos, Ernakulam, Supporting Phase 3 & 4 clinical trials. Assisting in CRF & ICF preparation and review. Patient screening and informed consent support. EDC entry using REDCap, Medidata Rave, Clinion. Managing IP accountability and site documentation. Ensuring audit readiness and GCP compliance. Coordinating with investigators and site teams.

Education

Bachelor of Science - BS, Biotechnology, MES College Marampally

International Institute of Clinical research and Healthcare, NCARF, Ernakulam