ACR 105
Clinical Research Capstone
- Total Units :
- 3.0
Available Classes
Online
Sep 09, 2024
to Dec 01, 2024
Section: C21
$952.83
Online
- Section:
- C21
- Class Semester:
- Fall 2024
- Cost:
- $952.83
- Date Range:
- Sep 09, 2024 - Dec 01, 2024
- Class Dates:
- No Scheduled Class Meetings, September 9 - December 1 (Online)
- Location:
- ONLINE
- Instructor:
- Lawrence Reiter
- Notes:
- ACR 104 is a co-requisite to this course. You must either have completed ACR 104 or be enrolled in ACR 104 at the same time as completing ACR 105. This capstone is a team-based course operationalizing a clinical trial. Webinars will be hosted on Wednesdays from 7:00pm to 9:00pm on the following dates: October 5, October 26 and November 23. Webinars will be recorded. During the week of December 12, a mandatory webinar assignment will take place. Teams will schedule a day and time with the instructor at the beginning of the course. Please note registering after the course start date may delay course access and does not permit exceptions to coursework due dates, late textbook purchases, or the refund policy.
Online
Jan 13, 2025
to Apr 06, 2025
Section: C21
$952.83
Online
- Section:
- C21
- Class Semester:
- Winter 2025
- Cost:
- $952.83
- Date Range:
- Jan 13, 2025 - Apr 06, 2025
- Class Dates:
- No Scheduled Class Meetings, January 13 - April 6 (Online)
- Location:
- ONLINE
- Instructor:
- Lawrence Reiter
- Notes:
- ACR 104 is a co-requisite to this course. You must either have completed ACR 104 or be enrolled in ACR 104 at the same time as completing ACR 105. This capstone is a team-based course operationalizing a clinical trial. Teams will schedule a day and time with the instructor at the beginning of the course to meet, these meetings are maditory to attend for the success of the capstone. Please note registering after the course start date may delay course access and does not permit exceptions to coursework due dates, late textbook purchases, or the refund policy.
Instructors
Lawrence Reiter
Lawrence Reiter has almost 20 years’ experience in the Pharmaceutical Research Industry in Clinical Operations, Project Management, Quality Assurance and Compliance. His experience includes monitoring and project management across a wide variety of therapeutic areas to include drug and device studies across all phases.
Lawrence has worked in multiple regions around the world and manages global studies in over 40 countries. In addition, he is accredited by and remains in good standing with the Society for Quality Assurance as a Registered Quality Assurance Professional in Good Clinical Practice (RQAP-GCP).
Lawrence is an experienced lecturer in GCP having been directly involved in the setup and running of a non-profit training organization in South Africa that provided training across global regions to both Sponsor and site staff.