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CRC Intern | EDC & Clinical Documentation | B.Pharm | GCP Certified

About

B.Pharm graduate currently working as Clinical Research Coordinator (CRC) Intern with an exposure to clinical trial operations, patient coordination, study documentation and Electronic Data Capture (EDC). My experience includes EDC data entry, query resolution, source document maintenance, tracking patient visits, protocol review, sample processing and laboratory documentation. As a Backup CRC I assist with multiple regulatory and non regulatory studies ensuring study protocol and GCP compliance. I have hands-on experience in eTrialTrack and Clinivigilant eClinical platforms including patient recruitment, inclusion/exclusion criteria, randomization documentation, and clinical data process. Pharmacovigilance trained, GCP Certified, Strong foundation in ICH-GCP, Clinical Documentation, Patient Safety, Study Compliance. Currently seeking opportunities in Clinical Research, Clinical Trial Coordination, Pharmacovigilance, and Drug Safety. Open to opportunities across the Mumbai Metropolitan Region (MMR).

Location

Mumbai

Work experience

clinical research coordinator intern at Thrive clinical research service, Apr 2026 - Present · 3 mos, Kalyan Dombivli, Maharashtra, India, • Supporting clinical trial activities and patient coordination. • Performing EDC data entry and assisting with query resolution. • Maintaining study documents, screening records, and patient visit schedules. • Reviewing study protocols and understanding patient eligibility criteria. • Processing laboratory samples and supporting study documentation. • Working as a Backup CRC across multiple clinical studies. • Following ICH-GCP guidelines and ensuring accurate clinical documentation.

Registered Pharmacist at Bhawani Medical General Store, Jun 2024 - Mar 2026 · 1 yr 10 mos, Mumbai, Maharashtra, India, Managing 200+ daily prescription records with zero documentation errors—applying the same SOP-based verification discipline that clinical trial sites use every day. Built audit-ready filing systems comparable to Investigator Site File standards. Handle direct patient interactions daily, which has sharpened my communication skills for informed consent and subject follow-up processes. Monitor medication safety concerns regularly, reinforcing practical awareness of adverse event identification and reporting.

Industrial Exposure – Clinical Research Coordination at Bio-Prospera Clinical Research Pvt Ltd., Feb 2026 - Feb 2026 · 1 mo, Vasai, Maharashtra, India, Gained direct hands-on exposure to site-level clinical trial operations at a functioning CRO. Observed how coordinators manage regulatory documentation, maintain study files, and ensure protocol compliance in a real clinical trial environment. Developed practical understanding of CRO workflows, site management processes, and ICH-GCP documentation standards that no classroom training can replicate.

Member at PHO Cell Member, 2022 - Jan 2024 · 2 yrs 1 mo, Mumbai Metropolitan Region, Led public health awareness campaigns on STI disease prevention, stem cell donation, and folic acid supplementation. Developed patient communication, community outreach, and health education skills directly relevant to clinical trial subject recruitment, informed consent processes, and patient retention in clinical research settings.

Intern – Analytical & Formulation Department at Sun Pharma Advanced Research Company Pvt. Ltd., Mumbai, Jun 2023 - Jun 2023 · 1 mo, Andheri, Completed internship at one of India's leading pharmaceutical R&D companies. Observed and supported GxP-compliant SOP-based documentation and quality-controlled pharmaceutical processes within a regulated research environment. Built foundational understanding of the compliance and documentation standards that directly govern clinical research and CRO operations.

Education

Bachelor of Pharmacy (B.Pharm), Pharmacy, Vivekanand Education Societys College of Pharmacy Sindhi Society Chembur Mumbai 400 071