Molgara Keerthi
Clinical Research Coordinator Intern
HyderabadMember since June 17, 2026
ICH-GCPInformed Consent ProcessSubject RecruitmentRegulatory DocumentationCRF ManagementSource DocumentationEDCCTMSAE/SAE ReportingPharmacovigilanceData ManagementMS OfficeiMedidata RaveResearch ManagerVeeva VaultCenduitALMAC4G IRTZelta
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About
Pharm.D graduate with hands-on experience in clinical research coordination, clinical trial conduct, patient management, regulatory documentation, informed consent, adverse event reporting, and data quality. GCP-certified professional seeking opportunities as a Clinical Research Coordinator.
Experience
Clinical Research Coordinator Intern - Yashoda Healthcare Services Limited - Hyderabad
(2025-06 - 2026-05)
- Coordinated Phase I–IV clinical trials in compliance with ICH-GCP guidelines.
- Managed informed consent, participant screening, enrollment, and follow-up visits.
- Maintained source documents, CRFs, and EDC systems with high data accuracy.
- Supported regulatory submissions, monitoring visits, audits, and inspections.
- Tracked and reported adverse events (AEs/SAEs) according to protocol timelines.
- Collaborated with investigators, sponsors, CROs, and study monitors.
Education
Doctor of Pharmacy - Pharmacy - Avanthi Institute of Pharmaceutical Sciences (2020 - 2026)
Skills
Clinical Research Coordinator Intern
