Director of Clinical and Regulatory Services @ Enmed (February 2000 - May 2001)
Clinical Project Manager @ (November 1998 - January 2000)
Senior Clinical Research Associate @ Transcend Therapeutics (November 1997 - November 1998)
Medical Research Associate @ (June 1996 - December 1997)
Clinical Study Coordinator and Biomedical Data Specialist @ (January 1995 - June 1996)
Clinical Project Leader Phase 1 Unit @ Medical and Technical Research Associates (August 1993 - December 1994)
Rita Pease Education
University of Massachusetts Lowell 1989-1993
Rita Pease Skills
21 CFR Part 11
Biotechnology
CRO
CRO Management
CTMS
Clinical Development
Clinical Research
Clinical Study Design
Clinical Trials
FDA
GCP
Medical Devices
Pharmaceutical Industry
Pharmaceutics
Quality Assurance
Quality System
Regulatory Affairs
Regulatory Submissions
SOP
Standard Operating Procedure (SOP)
Management
Process Improvement
Training
Rita Pease Summary
Rita Pease, based in Boston, MA, US, is currently a Quality Assurance Compliance Associate at Harbor Clinical. Rita Pease brings experience from previous roles at Harbor Clinical, Synspira and Pease GCP Compliance. Rita Pease holds a 1989 - 1993 University of Massachusetts Lowell. With a robust skill set that includes 21 CFR Part 11, Biotechnology, CRO, CRO Management, CTMS and more. Rita Pease has 2 emails on RocketReach.
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