Jenisha Mary

Jenisha Mary has over 8 years of experience in regulatory submission publishing, currently serving as a Regulatory Associate at Navitas Life Sciences since December 2020. Previously, Jenisha worked as a Regulatory Affairs Trainee, gaining expertise in various regulatory submissions such as IND, ANDA, NDA, and DMF in eCTD formats for multiple health agencies, including US-FDA and EMA. Jenisha's experience also includes a role as a Clinical Research Coordinator at Chettinad Hospital and Research Institute, where involvement in a clinical trial for herbal formulations highlighted strong skills in planning, design, development, reporting, and analysis. Earlier experience as a Student Intern at AZIDUS Laboratories involved participating in a BA/BE study of Pinaverium Bromide, focusing on volunteer management and protocol preparation. Jenisha holds a Master's degree in Clinical Research, Experimental Medicine from Chettinad Hospital and Research Institute, along with a Bachelor's degree in Physician Assistant from India Heart Foundation, Chennai.