12-Hour Clinical Trial Management Series

Jun 10, 2020, 21:35 PM
Course ID : 276
Acronym : CTMS
Improve key skills of clinical trial management with Barnett International's course. This program covers risk analysis, regulatory submissions, and site selection techniques. Enroll today!

Course Description

The 12-Hour Clinical Trial Management Series will focus on the critical skills needed for successful clinical trial management. This series is geared toward clinical trial managers, clinical project managers, and other key trial personnel seeking to improve their trial management expertise. Each module will focus on a comprehensive competency for clinical trial managers and project managers, as described in the learning objectives and course modules. Clinical trial management skills are reinforced through a combination of activities, including case studies and scenario review.

Prior to the start of the course, participants will receive their login credentials and links to access and download the many class resources and class meeting links. Upon course completion, participants will be provided training certificates. In order to receive accreditation CEUs, participants are required to pass a final exam. Upon completion of the exam, CEU certificates will be provided.

Learning Objectives

  • Understanding risk and risk analysis for clinical trials
  • Identify effective vendor selection, oversight and risk management techniques
  • Apply risk management techniques in protocol development, site selection, and vendor selection
  • Develop effective budgets for clinical trials
  • Describe useful metrics and forecasting techniques used in clinical trials
  • Describe strategies for effective communications and meetings

Course Outline

  • Module 1: Risk Management Part 1: How Clinical Trial Managers are Risk Managers Throughout the Project Lifecycle 
  • Module 2: Vendor Management and Selection: Effective Selection, Oversight and Risk Management of Clinical Trial Vendors
  • Module 3: Risk Management Part 2: Application of Risk Management
  • Module 4: Budget Management: Successful Budget Planning and Management
  • Module 5: Metrics and Forecasting: Why Metrics and Forecasting Matter in Clinical Trials
  • Module 6: Effective Communication and Meetings

Who Should Attend

  • Clinical Trial Managers
  • Clinical Project Managers
  • Clinical Research Department/Team Managers
  • Clinical Research Associates and others seeking a better understanding of clinical trial management

NOTE: This course is for individual registrants only and does not allow for group training.

What participants say about Barnett's 10-Week courses ...

“Great course! Instruction is expertly led and engaging. I will recommend Barnett to any colleague and will seek out topics for my own future training and professional development needs.”

"The course has been so incredibly helpful thus far...I look forward to Thursday evenings!"

“This class exceeded my expectations of an online learning experience. The instructor was knowledgeable, came equipped with great examples to keep the class interesting and is a strong presenter. Thank you!”

Instructor

Shana Zink, B.S., C.C.R.A.

Click here for complete trainer biographies

Course Length and Time

2 hours/week for 5 weeks.

Registration Fees

$1,595 by Early Bird Deadline

$1,795 after Early Bird Deadline

This course is for individual registrants only and does not allow for group training.

All participants are eligible for “Certificates of Attendance,” and accreditation, provided that accreditation requirements are met.

Accreditation Information

Barnett International is accredited by the Accreditation Council for Pharmacy Education as a provider of continuing pharmacy education.  Participants will receive 12 hours (1.2 CEUs) of continuing education credit for full participation, including the completion of a final exam, and program evaluation.  Barnett International will issue a receipt of completion for earned CEUs within three weeks of program completion.  ACPE#: 0778-0000-23-044-L99-P. Released: 7/23.  

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

Series :
  • Clinical Trials & Translational Medicine
Topics :
  • Clinical Research
Job Functions :
  • Clinical Operations & Trial Management
  • Clinical Quality Assurance
  • Clinical Research Associate
  • Clinical Research Coordinator
  • Clinical Research Investigator
  • Data Management
  • Drug Safety
  • Medical Affairs
  • Project Manager
  • Quality Control
  • Regulatory Affairs
  • Study Site Compliance
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