Certificate in clinical trials management

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This certificate requires an application before taking any courses. View the complete Certificate Registration and Candidacy Guidelines. Develop substantive knowledge about coordinating and managing a clinical trial, including the drug development process, human subjects protection, working with institutional review boards IRBs , and application of good clinical practice regulations and guidances from both FDA and ICH perspectives.

Learn how to set up a new clinical study; how to monitor clinical trials; as well as when, why, and how to engage clinical research organizations CROs.

Build or reinforce essential skills, such as data management, site and investigator recruitment, and project management. Discover a new understanding of oncology clinical research, from the basic science of cancer, to monitoring oncology trials. Gain an overview of the entire clinical research process to identify the various career paths within the industry. Managers in training and others who want to refine or update skills Research associates and coordinators Biomedical and research scientists Nurses and allied health professionals Statisticians and database administrators International clinical trials professionals Individuals with degrees in science, psychology or related areas who are entering the field.

Format: Online In-class options might be available for some courses. Duration: 6 - 24 months Varies by student and courses taken per quarter. Courses Delivery Method Show Legend. Units: 1. See Details. Required Courses. Units: 3. Upcoming Start Dates: January 3, Units: 2. Upcoming Start Dates: January 31, Upcoming Start Dates: January 18, Electives 14 units are required. Upcoming Start Dates: January 11, Typically Offered: Winter, Summer. Upcoming Start Dates: April 10, Typically Offered: Spring.

Upcoming Start Dates:. Upcoming Start Dates: October 18, Typically Offered: Fall, Spring. Upcoming Start Dates: January 10, Regulatory Topics.

Upcoming Start Dates: February 22, Upcoming Start Dates: January 10, April 4, Project Management topics for sponsors of clinical trials. The curriculum of the Clinical Trials Management Online Certificate covers core concepts consistent with the Association of Clinical Research Professionals ACRP certification exams, a valuable credentialing opportunity for clinical research professionals.

For exam details, including eligibility requirements, visit Association of Clinical Research Professionals. Her roles have included director of a field-based regional monitoring program and senior director of clinical study management, where she was responsible for management of in-house staff and accountable for the delivery of clinical trials across multiple therapeutic areas.

Prior to her career in the pharmaceutical industry, she practiced as an RN in various clinical agencies and taught nursing in academia. New for spring ! To earn the Clinical Trials Management Certificate, all three of the following modules must be successfully completed with a passing grade 60 or higher and earn an overall final grade for the certificate of 70 or above.

This module provides an overview of the clinical and pre-clinical processes involved in setting up clinical trials, and the roles and responsibilities of those conducting and administering these processes. Topics include:. This module focuses on the processes involved in conducting safe, thorough, and reliable clinical trials.

This module focuses on the steps necessary for completion and evaluation of clinical trials processes. For details, contact Wilmington University at coel wilmu. In addition, two years of college level coursework is recommended. Ready to take your next step? How to Apply Contact Us. Healthcare Rapid changes in medicine and biotechnology are creating a new understanding of pathology, health, and well-being. Learn more about Healthcare. Of Interest. Story March 26, Clinical Trials Management and Regulatory Compliance.

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