The Complete Faculty Roster
Bridging international regulatory best practices with Central India's clinical research trial sites.
Mr. Chetan Ingale
TCSGeneral Manager (Pharmacovigilance)
Leadership in enterprise pharmacovigilance operations, global aggregate safety reports, signal management, and ICSR regulatory reporting workflows.
Mr. Adarsh Sharma
IQVIASr. GM – Clinical Trials & Global Operations
Oversees multinational Phase II–IV clinical trials, risk-based monitoring (RBM) frameworks, site feasibility, and global audit readiness.
Mr. Rahul Dhamat
NovartisSr. Manager – Clinical Data Management (CDM)
Expert in electronic data capture (EDC), clinical database design, data validation specifications (DVS), and CDISC SDTM mapping for global trials.
Dr. Vishal Pendharkar
Cambridge, UKDrug Discovery Leader & Research Scientist
Translational research specialist connecting early chemical discovery, target identification, and European clinical biotechnology pipelines.
Mr. Ahmad Aziz Khan
Reliance, MumbaiProject Manager – Clinical Operations
Veteran clinical trial project manager with extensive experience in multicenter clinical trial execution, site contracts, and budget governance.
Mr. Onkar Rathod
Glenmark PharmaceuticalsDy. GM – Clinical Research & Regulatory
Senior pharmaceutical executive leading bioequivalence studies (BA/BE), USFDA/EMA regulatory submissions, and GCP protocol adherence.
Mr. Akash Dhokne
GermanyClinical Research Professional
European clinical operations practitioner specializing in EU CTR regulatory transitions, cross-border monitoring, and clinical audit readiness.
Kate Savenko
Vinnytsya, UkraineExpert – CDM, Clinical Trials & EDC
Specialized in Medidata Rave, Oracle InForm, electronic Case Report Form (eCRF) design, discrepancy resolution, and database lock.
Iva Sabeva
BulgariaClinical Research Coordinator (CRC)
Experienced site coordinator guiding scholars through patient screening, source data verification (SDV), and trial master file compliance.
Irene Uclés
Barcelona, SpainCRA – Early Clinical Development
Focuses on early-phase oncology protocols, dose-escalation safety monitoring, and ICH E6(R2) monitoring trip reports across European clinical sites.
Jasmina Deisting
Stralsund, GermanyCRA | Certified EU Clinical Trials PM
Certified European Clinical Trials Project Manager guiding complex multi-country trial setup, regulatory dossier submissions, and risk management.
Tin (Tim) Hoang Trung
Ho Chi Minh City, VietnamClinical Research Coordinator (CRC)
Asia-Pacific clinical operations specialist coaching students on trial logistics, investigator site file management, and patient retention strategies.
Mr. Kunal Kumar
IQVIATeam Manager – Patient Safety Solution (PV)
Leads clinical safety adjudication panels, serious adverse event (SAE) processing, and pharmacovigilance data harmonization workflows.
Alicja Więcek
Łódź, PolandClinical Trial Coordinator | Biotechnology
Combines medical biotechnology and trial coordination expertise, focusing on biological specimen collection, lab kits, and clinical protocol adherence.
Weronika Krakowska
PPD, PolandClinical Research Associate I (CRA I)
Conducts site qualification visits, initiation visits, source document verification, and investigator compliance oversight for international CRO studies.
Learn from the Leaders Shaping the Future of Medicine
Get direct access to masterclasses, live Q&A sessions, and 1-on-1 career coaching with our global faculty.
Explore Courses & Join a Cohort