Barnett International's Core Curriculum courses are comprehensive role-based clinical research training programs designed to provide industry professionals with hands-on training in a dynamic virtual setting. Held four times a year during our “Clinical Research Training Weeks,” courses offer clinical research-focused, performance-based training and core competency development.
Advanced Clinical Research Coordinator (CRC) Training
Upcoming Courses
This refresher course provides additional training for the clinical research coordinator (CRC) with greater than three years of experience. We will start out with a review of the key governing regulations and guidelines in clinical research, and will then discuss trends, management issues and the financial impact of clinical research on the research site. We will also cover inspection preparation, as well as CAPA planning and implementation. This course will also focus on investigator responsibilities and developing processes that will ensure adequate investigator oversight.
- Understand the relevant regulations and guidelines
- Discuss trends in clinical research
- List and prioritize study management activities
- Discuss study management issues
- Describe financial impact and trends
- Prepare for an inspection
- Develop Corrective and Preventive Actions Plans (CAPA)
- Ensure adequate training and documentation of training of clinical research staff
- This course has been developed for the individual, CRC, nurse coordinator, Site Manager, investigator who has a solid background in the CFRs, ICH E6 Guidelines, and either involved in or manages the daily operation of clinical research at a trial site. This course can be beneficial to the CRA and members of the sponsor/CRO industry.
The course will be led by one of the following instructors:
Nikki Christison, B.S., C.C.R.A.
Lily Romero, P.A. C.C.R.C.
Click here for complete trainer biographies
Day 1: 8:30 a.m. – 5:00 p.m.
- Recap, including updates, of CFRs, ICH, GCP and relevant guidance documents
- Trends and changing landscape in clinical research
- Study Management: Prioritizing
- Study Management: Financial
- Training the Clinical Research Staff
- FDA inspections/Preparing for an Inspection
- Corrective and Preventive Action Plans/ Case Study
- Case study
- Case Scenarios, case study and site priorities exercises are among the scheduled activities in this interactive class
Registration fees include assorted breakfast items that will be available each day ½ hour prior to the start of the seminar. Also included is a Networking Lunch that will be served each training day.
Special rates are available for multiple attendees from the same organization. Contact Melissa Dolen at 781-972-5418 to discuss your options and take advantage of the savings.
Click here for our seminar cancellation policy
Barnett International is accredited by the Accreditation Council for Pharmacy Education as a provider of continuing pharmacy education. Participants will receive 7 hours (0.7 CEUs) of continuing education credit for full participation, including the completion of a pre-test, post-test and program evaluation. Barnett International will issue a receipt of completion for earned CEUs within three weeks of program completion. ACPE# 0778-0000-15-001-L01-P. Released: 4/15.
Hold this course at your company!
For more information, contact Naila Ganatra at (215) 413-2471.
