Monitoring Reports: 10 Rules of Effective Report Writing

Oct 6, 2018, 18:20 PM
Course ID : 052
Acronym : RWR
Get pro tips for effective report writing with Barnett International's course. Elevate your CRA career. Learn more today!

Course Description

The Clinical Research Associate (CRA) creates reports that have many audiences, one being regulatory authorities reviewing essential documentation of clinical trials linked to marketing application approvals. This web seminar presents 10 categories of scientific report writing in the context of the role of the CRA and the reports that they write. The applicable reports are monitoring visit reports, e-mails, telephone reports, Memos to File, and more. The concepts of writing in a scientific voice versus first person, objective versus subjective, and many more are presented. This course is invaluable for the CRA, as well as the individual who critiques the various reports.

Learning Objectives

  • Examine the impact of poor report writing
  • Apply the definitions and concepts of scientific report writing
  • Implement the 10 rules of quality report writing for CRAs
  • Apply the 10 rules to CRA activities
  • Write action items, deviations, queries
  • Integrate essential document mapping within a monitoring report
  • Describe the challenges of CRA report writing and report review

Who Should Attend

  • Clinical Research Associates
  • Contract Clinical Research Associates
  • Clinical Research Associate Managers
  • Project Managers

Instructor

Janet Ellen Holwell, C.C.R.C., C.C.R.A., T.I.A.C.R., F.A.C.R.P.

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 3 hours (0.3 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#: 0778-0000-22-014-L04-P. Released: 2/22.  

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
  • Project Manager
  • Regulatory Affairs
  • Study Site Compliance
  • Training
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