Dattatrya Kankatte
M.Pharm (Pharmacology) graduate with clinical research internship experience
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About
M.Pharm (Pharmacology) graduate with 3 months of clinical research internship experience and knowledge of regulatory documentation, ICH-GCP guidelines, clinical trial processes, and compliance requirements. Familiar with maintaining Trial Master Files (TMF), case report forms (CRFs), and accurate study records. Seeking an entry-level Regulatory Affairs role to support regulatory submissions, documentation review, and compliance activities.
Experience
Clinical Research Coordinator (CRC) - Proclin Research Private Limited - Bengaluru, Karnataka
(2026-01 - 2026-05)
- Assisted with clinical trial coordination in accordance with study protocols, ICH-GCP guidelines, and regulatory requirements.
- Collected, recorded, and maintained patient data and case report forms (CRFs) with accuracy and confidentiality.
- Supported participant recruitment, screening, informed consent, and scheduling of study visits.
- Coordinated communication among investigators, sponsors, monitors, and study participants to support smooth site operations.
- Maintained Trial Master File (TMF) records and supported Site Initiation Visits (SIV), Site Monitoring Visits (SMV), AE/SAE reporting, and study close-out activities.
Education
Master of Pharmacy - Pharmacology - BLDE Association's SSM College of Pharmacy (2025-11)
Bachelor of Pharmacy - KLE College of Pharmacy (2023-06)
