Hotel Information:
Marriott Residence Inn Arlington at Rosslyn
Marriott Residence Inn Arlington at Rosslyn
1651 N Oak Street
Arlington, VA 22209
Discounted Hotel Room Rate: $229.00
Reserve Your Hotel Room: Call hotel and mention PERI to receive discounted rate.
Deadline to Receive Discounted Rate: 1/23/08
Rate: $
229
Deadline for Group Rate:
2008-01-23
Hotel Policy
|
Registration Rate:
$1,495.00 Register by 12/31/07
$1,695.00 Register after 12/31/07
Cancellation Date: 1/28/08 (Cancellation fee is determined by date cancelled.)
Course Completed
Registration Policy
Continuing Education Credit:
ACPE:
708-000-07-037-L03 (18.75 CEU)
Initial Release Date:
5/7/07
CBRN:
N/A
CME:
18.75 Hours of Category 1 Credit
VNA:
07-04-01 18.75 Contact Hours
Continuing Education Policy
|
| |
Course Description:
Course is being held at:
PERI Training Facility
1616 N Fort Myer Drive
Suite 1430
Arlington, VA 22209
This course provides an overview of the clinical trial process with particular emphasis on planning and management. A balanced presentation of process and opportunity for detailed discussion and networking will address specific situations that impact efficiency, cost, and study completion. Interactive sessions serve as the basis for thoughtful analysis of how to design effective and efficient studies.
|
Who Should Attend:
This course is intended primarily for those involved in planning and management of multiple clinical trials. Team members who should attend include clinical research associates, study coordinators, medical program coordinators, clinical research managers, clinical affairs specialist, project managers, medical services managers, medical research associates, clinical/principal investigators, and clinical/medical monitors.
|
Educational Objectives:
Upon completion of this course, participants should be able to:
- Describe the principles and processes related to clinical trial effectiveness.
- List essential elements of protocol development.
- Identify effective patient recruitment resources.
- Assess staff and outsourcing needs to meet the changing needs of clinical trial management.
- Manage sponsor-CRO relations more effectively.
|
Key Topics:
- Key Success Factors in Managing Clinical Trials
- The Drug Development Process
- Developing Safe, Effective and Efficient Biologics
- The Clinical Trial Checklist
- Project Management
- Study Recruitment and Working with Sites
- Investigators' Meetings
- Institutional Review Boards (IRBs)
- Managing Outsourcing
- Case Report Form Development
- Data Collection and Electronic Data Capture
- Drug Development Workshop
|
|
Contact Course Manager:
Course Manager
|
| |
|
|
|
PERI reserves the right to change agenda
items and instructors without notice to accommodate
situations beyond its control.
|
