Entry Level Clinical Trial Monitoring (Clinical Research Associate) Course

Entry Level Clinical Trial Monitoring (Clinical Research Associate) Course

We are pleased to announce Entry level Clinical Trials Monitoring Course offered by ClinWin Research Services in partnership with KAVI Institute of Clinical Research, Department of Microbiology, University of Nairobi. The course will be held on 07 -12 October 2019, Nairobi, Kenya.

Introduction:

Clinical Research Associate (CRA); also, commonly known as a monitor supervises, monitors, and supports the administration and progress of a clinical trial on behalf of a sponsor. The sponsor, whose intent is the research of pharmaceuticals, biologics, or devices, may employ these individuals either directly or indirectly via contract research organizations (CROs), or as independent consultants or contractors.

Who should attend?

The course is designed for individuals with at least two years’ work experience in clinical research work at Investigator site level, Sponsor (academic, Pharmaceutical or not for profit research organizations) or related health care industry.

Course Cost and Scholarship

The cost of the training is Ksh 100,000 (Hundred thousand), to cater for the course materials, lunch, morning and afternoon tea and Certificate. We will offer partial scholarship for 2 participants to cover for the tuition fee to eligible applicants. Please indicate need and send us motivation letter detailing the potential future impact of this course to your career progression.

The training fee payment account.

Account name:                Clinwin Research Services

Bank:                                    Stanbic Bank , Upper hill branch

Account number:              0100003072015

Swift Code:                         SBICKENX

The training fee should be paid on or before 30 September 2019. Please email us the payment confirmation once done.

Course Certification

The training is organized in collaboration with University of Nairobi, KAVI Institute of Clinical Research. The training involves classroom presentations, practical’s and group discussions. Pre and post course assessments will be administered.

The participants will be issued with Certificate of Completion upon successful completion of the course.

How to Register;

Send us an email and brief CV to: training-coordinator@kaviuon.org and copy info@clinwinresearch.com

Pre-course work

Find below links to essential trainings, please register, complete the trainings and email me certificates on or before 30 September  2019.

1. Introduction to clinical research
2. ICH GCP (R2)
3. Research Ethics
4. Informed Consent
5. Introduction to Collecting and Reporting Adverse Events
6. How to Conduct GCP Inspections/Audits at the Clinical Investigator Site 
7. Introduction to Data Management For Clinical Research Studies 
8. Ethics and Best Practices in Sharing Individual-Level Research Data 
9. Responsible Conduct of Research 

https://about.citiprogram.org/en/homepage/

https://elearning.trree.org/

https://globalhealthtrainingcentre.tghn.org/elearning/short-courses/

http://ocw.jhsph.edu/index.cfm/go/viewCourse/course/drugdevelopment/coursePage/assignments/ – follow this and read materials on Principles of Drug Development

https://myscrs.org/tc_sqt/modules/12_Monitoring-%26-Auditing/story_html5.html