Bedanta Chetry
A lifelong learner | Clinical Operations - Cardio & Oncology | ICH GCP E6R3 | NDCT19 | MDR17 | Passionate about clinical research and trials in pharmaceuticals & medical devices | Aspiring opportunities.
- Role
- Clinical Trial Assistant at Clicebo Solutions Private Limited
- Location
- South Delhi, DL, IN
- LinkedIn followers
- 500 followers
About Bedanta Chetry
Currently working as a Clinical Trial Assistant on a cardiology project. Starting with a passion for patient-centered care, I began my professional journey as an Oncology Data Analyst at Navya Network. Life intervened when I became a full-time caregiver during a family health crisis and a series of unforeseen events, pressing pause on my career but accelerating my empathy and resilience. During this period, I stayed engaged through ICMR-NIE and NIH certifications and ISCR webinars, ensuring my regulatory knowledge and clinical acumen only deepened. & : As an Oncology Data Analyst, I curated EHR datasets, generated FAERS/EVDAS safety reports, and optimized NCCN-aligned oncology protocols. Supported Phase site initiation, CRF management, and ISF as a Clinical Trial Coordinator Trainee; executed NABL-accredited diagnostics and upheld SOP compliance as a Medical Lab Technologist Intern. With an MSc in Clinical Research, I mastered ICH-GCP trial design, protocol, CSR, eCTD regulatory writing, pharmacovigilance, protocol development, and a PCOS biomarker dissertation showcasing study design and scientific writing: Clinical Trial Management (Phase I–IV): site initiation, monitoring, TMF/EDC compliance. Medical & Scientific Writing: CSRs, CTD modules, manuscripts, SOPs (ICH E3). Pharmacovigilance & Drug Safety: ICSR, MedDRA, CIOMS, and SAE reportings. Oncology Protocols & Guidelines: NCCN adherence, RECIST, Real-world Evidence data. Regulatory Compliance: NDCT-19/MDR 2017/ICMR ethical guidelines. Accelerated Study Start-Up: Translate complex cardiology/oncology protocols into actionable CRO workflows. Data Integrity & Compliance: Ensure rigorous audit-readiness & trial records documentation. Efficient Regulatory Writing: Deliver timely IND/NDA dossiers aligned with global regulations. Patient-Centered Safety: Lead proactive signal detection and craft safety narratives that safeguard participants.I’m ready to drive quality, compliance, and speed—whether you’re in India or on a global remote/hybrid team. If you seek a resilient, scientifically rigorous professional who transforms challenges into strengths.’ - b••••••••@gmail.com |+91••••••••89
Experience
Clinical Trial Assistant
Clicebo Solutions Private Limited
Oct 2025 — Present · South Delhi, IN
Education
Padmashree Institute of Medical Lab Technology
Bachelor in medical lab technology, Clinical/Medical Laboratory Science/Research and Allied Professions
Rajiv Gandhi University of Health Sciences
MSc Clinical Research , Clinical Research
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