Dattatrya Kankatte

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.

Clinical Research Coordinator (CRC) at Proclin Research Private Limited (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.

Master of Pharmacy in Pharmacology – BLDE Association's SSM College of Pharmacy (2025-11)

Bachelor of Pharmacy – KLE College of Pharmacy (2023-06)