• SKIP TO CONTENT
  • SKIP NAVIGATION
  • Patient Resources
    • Clinical Trial Listings
    • What are Clinical Trials?
    • Become a Clinical Trial Volunteer
    • Useful Resources
    • FDA Approved Drugs
  • Professional Resources
    • Research Center Profiles
    • Market Research
    • Benchmark Reports
    • FDA Approved Drugs
    • Training Guides
    • Books
    • eLearning
    • Events
    • Newsletters
    • White Papers
    • SOPs
  • White Papers
  • Clinical Trial Listings
  • Advertise
  • Sign In
  • Create Account
  • Sign Out
  • My Account
Home » WIRB-Copernicus Group appoints Lindsay McNair chief medical officer

WIRB-Copernicus Group appoints Lindsay McNair chief medical officer

October 3, 2014
CenterWatch Staff

WIRB-Copernicus Group (WCG), a provider of regulatory and ethical review services and software to support clinical research, has promoted Lindsay McNair, M.D., M.P.H., M.S.B., to chief medical officer.

“As a physician, clinical investigator, consultant and former academic institutional review board (IRB) member, Dr. McNair brings her extensive experience of both drug development and the ethical oversight of research to our organization,” said Donald A. Deieso, Ph.D., WCG chairman and CEO. “With this powerful background, Dr. McNair will support WCG’s clinical professionals and clients in making decisions that create efficient and effective clinical development programs that respect and protect the well-being of clinical trial participants.”

McNair will guide the activities of more than 50 clinicians including physicians, nurses and biosafety experts. She has more than 15 years’ experience providing medical guidance on clinical development strategies and study designs for new drugs. In previous roles in the pharmaceutical industry, she has delivered medical oversight for all phases of clinical studies in a variety of therapeutic areas, including multiple oncology indications, hepatitis C, psoriasis and multiple sclerosis. In addition, Dr. McNair provides ethical guidance, having founded the Human Subject Protection Committee at Vertex Pharmaceuticals.

McNair is an adjunct associate professor at the Boston University School of Public Health, and was a member of the Boston University Medical Center IRB. She also is a member of The World Council for Ethical Standards; the Ethical Protocol Development Committee at the Multi-Regional Clinical Trials (MRCT) Center, which is administered by Harvard; the ethics committee for Care Dimensions, formerly known as the Hospice of North Shore and Greater Boston; and Public Responsibility in Medicine and Research (PRIM&R).

    Upcoming Events

    • 05Dec

      Thriving in Clinical Research – Overcoming Common Challenges as a Site: Part 3 – Site Resourcing

    • 14Apr

      MAGI 2024: The Clinical Research Conference

    Featured Products

    • Surviving an FDA GCP Inspection

      Surviving an FDA GCP Inspection: Resources for Investigators, Sponsors, CROs and IRBs

    • Best Practices for Clinical Trial Site Management

      Best Practices for Clinical Trial Site Management

    Featured Stories

    • Jonathan Seltzer

      Thought Leadership: Remote Patient Monitoring Gives New View of Safety in Cardiac Clinical Trials

    • Quality_Compass-360x240.png

      Ask the Experts: Applying Quality by Design to Protocols

    • Obesity Treatment Patient

      Clinical Trials Need Greater Representation of Obese Patients, Experts Say

    • Modernize-360x240.png

      FDA IT Modernization Plan Prioritizes Data-Sharing, AI, Collaboration and More

    Standard Operating Procedures for Risk-Based Monitoring of Clinical Trials

    The information you need to adapt your monitoring plan to changing times.

    Learn More Here
    • About Us
    • Contact Us
    • Privacy Policy
    • Do Not Sell or Share My Data

    Footer Logo

    300 N. Washington St., Suite 200, Falls Church, VA 22046, USA

    Phone 703.538.7600 – Toll free 888.838.5578

    Copyright © 2023. All Rights Reserved. Design, CMS, Hosting & Web Development :: ePublishing