CRC Advanced course
The CRC Advanced course is created for professionals with advanced training in a research field and provides students with the key skills, job criteria, and industry expectations for the positions of Clinical Research Coordinator and the critical role in the conduct of clinical trials.
This course is an addition to the beginner’s course and designed for persons with prior on-site clinical research experience, those who had a successful career in a healthcare field, and those with associate/bachelor’s degrees in a relevant field of studies seeking qualifications and/or current practical knowledge to effectively work within research industries.
Course outline:
- Principles of GCP
- Project Management for Clinical Trials
- Study Start Up
- Recruitment, Consenting, and Retention
- Trial Documentation
- Preventing and Identifying Misconduct and Noncompliance
- Safety of Subjects. AE, SAE reporting
- Training and Mentoring
- Financial Management of Clinical Trials
- Sponsor Responsibilities
- Preparing for Audit
Practical Strategies
This course will provide practical strategies for experienced CRCs to orient, train and supervise new CRCs, RAs, and MAs.
During the course you will learn the strategies of development of standardized orientation programs that cover essential topics. We will discuss continued training and professional development for experienced CRCs.
During the course of training students will participate in many simulation exercises that will expose you to actual trial situations with the Sponsors, PIs, CRAs, other clinical research professionals, and participants.
