Organization of Regulatory and Clinical Associates
P.O. Box 3490
Redmond, WA 98073
|
Current/Future Events - Event View
This is the "Event Detail" view, showing all available information for this event.
If the event has passed, click the "Event Report" icon to read a report and view photos that were uploaded.
An ORCA Lunch & Learn Event - Clinical Research Site Networks and Organizational Partnerships
About this event
TOPIC: Clinical Research Sites and Partnerships
TOPIC DESCRIPTION: Effective collaboration between clinical research sites, sponsor, and other vendors are critical to the success of clinical trials. Further efficiencies and collaboration between clinical research sites can lead to more efficient budgets, quicker timelines, and higher quality. Clinical research site networks these benefits through shared efficiencies and information.
SPEAKER: David Lew, MS, MBA
SPEAKER BIOGRAPHY: David is a strategic and collaborative leader with over 20 years of global experience in the clinical research industry across CRO, IRB, site, and sponsor organizations (including Covance, Fred Hutch, IQVIA, and PPD). His past experience includes Principal CRA, CTM, Sr. PM, and Sr. Director roles. He is currently Executive Director of Operations at Velocity Clinical Research. His involvement has been both high-level and hands-on in managing numerous early through late phase clinical trials across various therapeutic areas (including a strong focus on oncology) with consistent delivery of project, program, and organizational success.
David attended the University of Washington, where he earned a B.S. in Biology (Physiology), B.S. in Biochemistry (with a minor in general chemistry), and M.B.A. He also earned a M.S. in Biotechnology (with an emphasis in Regulatory Affairs) from the Johns Hopkins University, and a Certificate in Biotechnology Project Management from the University of Washington and University of California San Diego. He also holds current certifications from the ACRP (CCRA and ACRP-PM) and PMI (PMP). He was also a 2021 bronze award winner at the PharmaTimes Clinical Researcher of the Year competition.
WHO: Clinical, regulatory, quality, manufacturing and legal
Attendance at this meeting may be applied towards re-certification /continuing education from the following organizations:
| 1.5 pts |
RAC recertification from RAPS |
| 1.5 CEUs |
CCRP recertification from SOCRA |
| 1.5 CEUs |
CIP recertification from PRIM&R |
All attendees must be registered. Access to education content is a benefit of membership or guest attendance. The link to the webinar is intended for the registered person ONLY and any access/distribution of materials beyond the individual registrant is strictly prohibited. Viewing rights are not transferable and cannot be combined by multiple parties without express permission. Thank you for your understanding.
This webinar will be recorded.
Location
Webinar - Link will be emailed to attendees upon completion of registration.
USA
Registration Info
Registration is required before Friday, June 21, 2024 at 11:30 AM
Payment In Full In Advance Only
Registration closes 30 minutes before meeting start time.
Meetings and webinars are scheduled on Pacific Standard Time or Pacific Daylight Time, whichever applies.
Please make sure that the following email address is in your Safe Sender list: mailer@mail2.clubexpress.com. System messages like meeting announcements, registration confirmations, webinar login instructions as well as certificates of attendance are sent directly from this email address.
You will receive an email confirmation of your completed registration followed immediately by a separate email with the subject "Event Videoconference Notification." The Zoom link, Meeting ID, and Passcode for this webinar meeting will be in the second email. If you don't receive the instructions within this time frame, please contact us at info@orcanw.org as soon as possible.
PAID FEES ARE NON REFUNDABLE.
For webinar events, payment is REQUIRED at the time of registration.
 Invalid Quantity
|