ComplianceOnline

Understanding and Applying Best Practice Standards When Reviewing Clinical Research Contracts

Instructor: Jennifer Holcomb 
Product ID: 704337
  • Duration: 60 Min

recorded version

$249.00
1x Person - Unlimited viewing for 6 Months
(For multiple locations contact Customer Care)
Recorded Link and Ref. material will be available in My CO Section
Last Recorded Date: Jul-2016

Training CD

$299.00
One CD is for usage in one location only.
(For multiple locations contact Customer Care)
CD and Ref. material will be shipped within 15 business days

Customer Care

Fax: +1-650-565-8542

Email: customercare@complianceonline.com

Read Frequently Asked Questions

This training program will take an in-depth look at various clinical research contracts designed for different purposes. Understanding each type including what is being protected and who is being protected is an important part of ensuring compliant administration and management of clinical research activities. Beyond the legal terms, this course will examine the standards for accredited organizations and best practices for ensuring the broadest protections for study participants.

Why Should You Attend:

Understanding contract terms and provisions is essential to ensuring the interests of participants, sites and sponsors are detailed, agreed upon and protected. Contracts define everything from: who owns what data, who can use the data, what protections are offered in the event of injury to a participant to when and how payments are made and who is responsible for ensuring all compliance report criteria are met.

Clinical research contracts outline legal obligations of the study team and site, and legal limitations of protections, understanding these provisions leads to more effective communication between the business administrators responsible for oversight of the study and the legal representatives for the site and the sponsor who are responsible for negotiating terms.

This webinar will provide a robust knowledge of terms and understanding of common concerns as well as best practices in clear and understandable non-legal language. The instructor’s extensive knowledge and experience in clinical research administration, including contract review, and development makes her well suited to answer your questions and offer guidance in best practices for ensuring contracts are compliant with the highest standards of best practices.

Learning Objectives:

  • Identify each type of contract
  • Describe who is being protected
  • Understand provisions that comprise standard sections of a contract following best practice standards

Areas Covered in the Webinar:

  • Types of clinical research agreements
  • Elements of a CTA
  • Who is being protected and how
  • Understanding how contracts and protocols fit together
  • Who should participate in the review and why
  • When sites are non- profit, what differs

Who Will Benefit:

  • Investigators
  • Coordinators
  • Health System Administrators
  • Clinical Research Compliance Staff/ Officers
  • Industry Managers and Monitors
  • Business and Finance Administrators

Instructor Profile:

Jennifer Holcomb, MA, CCRC, is a clinical research professional with over 20 years of experience in the field. She is currently consulting privately. Ms. Holcomb has worked in nationally accrediting Institutions with AAHRPP. Her experience also includes serving in executive leadership roles at research institutions including Duke University, UCHealth System and University of Louisville. She provides guidance and leadership in the establishment and development of policies in the conduct and management of clinical research. Her key areas of expertise include clinical trial budgeting and contract negotiations as well as regulatory knowledge including international ICH GCP standards. Ms. Holcomb has extensive experience in training and education and served as Vice Chair of the ACRP Professional Development Committee for 4 years.

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Refund Policy

Registrants may cancel up to two working days prior to the course start date and will receive a letter of credit to be used towards a future course up to one year from date of issuance. ComplianceOnline would process/provide refund if the Live Webinar has been cancelled. The attendee could choose between the recorded version of the webinar or refund for any cancelled webinar. Refunds will not be given to participants who do not show up for the webinar. On-Demand Recordings can be requested in exchange.

Webinar may be cancelled due to lack of enrolment or unavoidable factors. Registrants will be notified 24hours in advance if a cancellation occurs. Substitutions can happen any time.

If you have any concern about the content of the webinar and not satisfied please contact us at below email or by call mentioning your feedback for resolution of the matter.

We respect feedback/opinions of our customers which enables us to improve our products and services. To contact us please email customercare@complianceonline.com call +1-888-717-2436 (Toll Free).

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