Sejal Batra, MS
Clinical Project Manager | Regulatory Affairs Expert
3 yrs experience · <10 hrs/week
About
With a Master of Science in Regulatory Affairs and Health Policy from the Massachusetts College of Pharmacy and Health Sciences, I have built a robust career in clinical project management. Currently serving as a Clinical Project Manager at PepGen, I oversee clinical trials, ensuring compliance with regulatory standards and managing project timelines and budgets. My previous roles include Associate Clinical Study Manager and Clinical Trial Associate at Codiak BioSciences, where I assisted in planning and executing clinical studies. I also held positions at TransMedics, Inc. and Catabasis Pharmaceuticals, Inc., where I supported clinical trial operations and monitored trials for data integrity and regulatory compliance. My educational background also includes a Pre-Medical and Health Studies degree from MCPHS and a high school diploma from Bishop Feehan High School.
Experience
- Clinical Project Manager · PepGen10-01-2023
As a Clinical Project Manager, likely responsible for overseeing clinical trials, ensuring compliance with regulatory requirements, and managing project timelines and budgets.
- Associate Clinical Study Manager · Codiak BioSciences07-01-2022 – 04-01-2023
As an Associate Clinical Study Manager, likely responsible for assisting in the planning, execution, and management of clinical studies, ensuring adherence to protocols and regulatory requirements.
- Clinical Trial Associate · Codiak BioSciences01-01-2022 – 07-01-2022
As a Clinical Trial Associate, likely responsible for supporting clinical trial operations, maintaining study documentation, and coordinating with study sites.
- Clinical Trial Associate · TransMedics, Inc.03-01-2021 – 12-01-2021
As a Clinical Trial Associate, likely responsible for supporting clinical trial operations, maintaining study documentation, and coordinating with study sites.
- Clinical Research Associate · Catabasis Pharmaceuticals, Inc.02-01-2020 – 10-01-2020
As a Clinical Research Associate, likely responsible for monitoring clinical trials, ensuring data integrity, and compliance with regulatory requirements.
Education
- Massachusetts College of Pharmacy and Health SciencesMaster of Science - MS, Regulatory Affairs and Health Policy
- Massachusetts College of Pharmacy and Health SciencesPre-Medical and Health Studies, Pre-Medical and Health Studies
- Bishop Feehan High School
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