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Maria Grasic Location
New York, NY, US
Maria Grasic Work
Associate Director, Risk Based Quality Management Lead @ (March 2025 - Present)
Clinical Data Scientist @ (June 2022 - January 2025)
Clinical Operations Lead @ (March 2021 - June 2022)
Lead Clinical Scientist 2 and Senior Study Lead (Dual Role) @ (May 2018 - March 2021)
Senior Central Monitoring Lead, Immuno-Oncology @ (November 2015 - April 2018)
Global Labeling Lead Manager, Oncology and Infectious Disease @ (September 2011 - November 2015)
Senior Clinical Protocol Manager, Oncology and Infectious Disease @ (May 2006 - August 2011)
Clinical Site Manager, Oncology @ (June 2003 - May 2006)
Project Manager Clinical and Regulatory Affairs, Diagnostic Devices @ (January 2000 - June 2003)
Medical and Cytogenetics Technologist @ (August 1994 - January 2000)
Maria Grasic Education
Northeastern University
Master of Science (M.S.) (Regulatory Affairs for Drugs, Biologics and Medical Devices)
Fairfield University
Bachelor of Science (B.S.) (Biology)
Maria Grasic Skills
Clinical Trials
GCP
Oncology
Pharmaceutical Industry
CTMS
Clinical Development
Clinical Research
Regulatory Affairs
FDA
Sop
CRO
Pharmacology
Medical Writing
Protocol
Therapeutic Areas
Drug Development
Clinical Operations
Clinical Monitoring
ICH-GCP
Biotechnology
Regulatory Submissions
Infectious Diseases
Pharmacovigilance
Biopharmaceuticals
Medical Devices
IND
Medical Affairs
Endocrinology
Regulatory Requirements
Clinical Data Management
Clinical Pharmacology
Hematology
Biologics
Oncology Clinical Research
Clinical Study Design
EDC
Oracle Clinical
21 CFR Part 11
Molecular Biology
Immunology
CRF design
Good Clinical Practice (GCP)
Standard Operating Procedure (SOP)
U.S. Title 21 CFR Part 11 Regulation
U.S. Food and Drug Administration (FDA)
CRO Management
Clinical Trial Management System (CTMS)
Clinical Trial Management System Ctms
Ich Gcp
Cardiology
Dermatology
Good Clinical Practice Gcp
Virology
Real Time Matching
Micro Classifieds
Clinical Trial Management
Lifesciences
Clinical
Clinical Trial
u.s. Food and Drug Administration Fda
Instant Virtual Marketplace
Vaccines
Diabetes
Oncology Clinical
Standard Operating Procedure Sop
Pharmacokinetics
Computer System Validation
Good Clinical Practice
Standard Operating Procedure
u.s. Food and Drug Administration
Clinical Trial Management System
Maria Grasic Summary
Maria Grasic, based in New York, NY, US, is currently a Associate Director, Risk Based Quality Management Lead at BeOne Medicines. Maria Grasic brings experience from previous roles at Arvinas, ICON plc and Bristol-Myers Squibb. Maria Grasic holds a Master of Science (M.S.) in Regulatory Affairs for Drugs, Biologics and Medical Devices @ Northeastern University. With a robust skill set that includes Clinical Trials, GCP, Oncology, Pharmaceutical Industry, CTMS and more. Maria Grasic has 1 emails and 1 mobile phone numbers on RocketReach.
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