Course Description

This course provides the background needed to become an integral part of the clinical research team (for drugs and devices) and explores the need to understand the rationale behind quality performance and team-playing. The roles and responsibilities of Clinical Administrative Support will be discussed in terms of obligations to the study team and the importance of compliance with Standard Operating Procedures and Standard Office Practices. Although the course is designed for administrative staff with less than one year experience, those with some experience may also find this course helpful in providing the rationale for doing tasks in a specific manner, refining their skills, and sharing their experiences and helpful techniques with their colleagues.

Learning Objectives

• Recognize the importance of a knowledgeable clinical support staff
• Define the common terms used in the field of drug and device research
• Describe the basics of the drug/device development process
• Describe the basic principles of Good Clinical Practice and the regulations that govern clinical research
• Discuss the basics of clinical trial design and use of a study protocol
• List essential Standard Operating Procedures needed
• Describe the responsibilities of various members of the clinical team
• List the essential documents needed for clinical trials and become familiar with the proper preparation of the documents needed to support the trial process
• Discuss the importance of training and maintenance of current training records
• Describe the rationale behind building quality into the filing system
• Discuss the “dos and don’ts” in the event of a regulatory agency audit

Who Should Attend

• Clinical Research Administrative Support Staff

Instructor

The course will be led by one of the following instructors:

Lily Romero, P.A., C.C.R.C.

Elizabeth Weeks-Rowe, LVN, C.C.R.A.

Click here for complete trainer biographies

Registration Fees

$835

Includes up to 20 participants at one site. All participants (up to 20) are eligible for “Certificates of Attendance,” and accreditation, provided that accreditation requirements are met. For groups larger than 20 or for additional sites, please call +1 781.972.5400 or toll-free in the U.S. 800.856.2556 for pricing.

Note: Due to COVID-19, we understand that most teams cannot currently dial-in together. As such, we are able to offer additional logins at a highly reduced rate. Please contact Barnett Customer Service at +1 781.972.5400 or toll-free in the U.S. 800.856.2556 to register with your additional participants requiring login credentials. Or email Customer Service at: customer.service@barnettinternational.com

Accreditation Information

Barnett International is accredited by the Accreditation Council for Pharmacy Education as a provider of continuing pharmacy education.  Participants will receive 2.5 hours (0.25 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#: 0778-0000-24-040-L99-P. Released: 9/24. 

Hold this course at your company! For more information, contact Naila Ganatra at +1 215.413.2471.