Senior Director, R and D QA @ (May 2020 - November 2023)
Director, Quality, Research @ (July 2018 - May 2020)
Director, Research Quality Assurance @ (February 2016 - July 2018)
Senior Consultant @ (April 2012 - February 2016)
Director, Quality Assurance @ (January 2004 - July 2011)
Manager, GCP Compliance @ (April 2001 - January 2004)
GCP Compliance Auditor @ (June 2000 - March 2001)
Quality Assurance Administrator @ (June 1999 - June 2000)
Quality Assurance Specialist @ (June 1998 - June 1999)
Senior Medical Technologist @ (June 1992 - May 1998)
Shift Coordinator, Transfusion Services @ (June 1992 - May 1994)
Roger Evans Education
University of Utah
Bachelor of Science
1990-1992
University of Utah
Master of Science (Psychology)
1986-1990
Colorado State University
Bachelor of Science (Psychology)
1982-1986
Roger Evans Skills
Clinical Development
21 CFR Part 11
GMP
GCP
Clinical Trials
GLP
Risk Management
Quality Auditing
CAPA
Regulatory Affairs
Quality Assurance
FDA
Biotechnology
Data Management
Pharmaceutical Industry
Sop
Validation
Change Control
GxP
Biologics
CRO
Drug Development
Clinical Monitoring
IND
Regulatory Submissions
Protocol
Computer System Validation
Oncology
Therapeutic Areas
Vaccines
Pharmaceutics
Quality System
Medical Devices
Technology Transfer
Pharmacovigilance
ICH-GCP
LIMS
Lifesciences
Regulatory Requirements
Quality Control
Biopharmaceuticals
GAMP
Clinical Data Management
EDC
Vendor Management
Vendor Audit
REMS
Risk Based Audits
Risk Assessment
PowerPoint
Sales
Hospitals
Ich Gcp
Roger Evans Summary
Roger Evans, based in Cambridge, MA, US, is currently a Senior Director Quality at Aditum Bio. Roger Evans brings experience from previous roles at Vor Bio, uniQure, Sage Therapeutics and Ironwood Pharmaceuticals. Roger Evans holds a 1990 - 1992 Bachelor of Science @ University of Utah. With a robust skill set that includes Clinical Development, 21 CFR Part 11, GMP, GCP, Clinical Trials and more. Roger Evans has 4 emails and 1 mobile phone numbers on RocketReach.
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