This capstone course is intended to simulate real-world experiences in the areas of clinical research protocols and study management. Working in teams, students will apply the theoretical knowledge and skills gained from previous courses in the program. Students will also be required to demonstrate successful study conduct using self-directed research, project management, and professional communication. Pre-requisite: ACR 104 Clinical Trial Management.
No Scheduled Class Meetings, January 13 - April 6 (Online)
Location:
ONLINE
Instructor:
Lawrence Reiter
Notes:
ACR 104 is a prerequisite to this course. 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 MANDITORY 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
People Card Modal Dialog
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.
