Elements of Clinical Study Coordination SCCR240

Course Information

Course Code

SCCR240

Instruction Method

Online – login information will be emailed on the course start date

Fee

Domestic $847 International $1101

Length

12 weeks – 4.8 CEUs

Instructor(s)

Faiza Khawaja

Learner Outcomes

By the end of the course, learners will be able to:

  • Explain the roles and responsibilities of a study coordinator
  • Describe the clinical trial budgeting and negotiation processes
  • Develop an effective recruitment plan
  • Identify the skills necssary to prepare sites to conduct clinical trials
  • Describe the steps and procedures involved in effective site management
  • Design and organize source documents  to meet protocol requirements
  • Describe effective methods for communicating with the REB and the sponsor
  • Identify steps to manage the final closeout and archive the study

Evaluation Method

Individual assignments, group case study, test, participation

Intended For

Healthcare professionals interested in clinical research


Note:

Course registration will close once maximum number of students enroll. Register as soon as you can!

Certificate Program

Clinical Research Program

Topics Covered

  • Introduction to Study Coordination
  • Financial Management of Clinical Trials
  • Site Management
  • Source Document Design and Organization
  • Pre-screening
  • Study Visits
  • Interaction with REBs and Sponsors
  • Study Close-out

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COVID Vaccine Requirement:

Effective September 7th all learners, faculty and staff must provide proof of at least one-dose of approved COVID-19 vaccine to participate in any in-person learning or on-site activities. Proof of full vaccination will be required as of October 8th, 2021.

Instructions to upload proof of COVID vaccination to Self Service


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