Bio
An expert in Clinical trial operations with more than 16 years of experience with various pharma industries and CROs in domains such as oncology, stem cell therapy in vascular surgery, orthopedics, and Diabetes research, etc. Have overseen and managed phase (I – IV) clinical trials, Medical Devices trials and BA/BE Studies.
Expertise in preparing protocols, Informed Consent Documents, Case Report Forms, SOPs and Manuscripts. Experienced in Regulatory Affairs, clinical data management, QA/QC activities, Medical Reporting and Documentation. Contributed as dynamic key person for the successful completion of 20 clinical trials across various domains.
