Course Announcement: 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 23 – 28 March 2020, Nairobi, Kenya.

Introduction

Clinical Research Associate (CRA); also, commonly known as a oversees the progress of a clinical trial, and ensures that it is conducted, recorded, and reported in accordance with the protocol, SOPs, Good Clinical Practice and applicable regulatory requirements. The Monitor provides operational and administrative support for the assigned clinical trial(s) projects 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

The cost of the training is Ksh 100,000 (Hundred thousand), to cater for the course materials, lunch, morning and afternoon tea and Certificate.

The training fee should be paid on or before 15 February 2020. Please email us the payment confirmation once completed.

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.

Pre-course work

The interested participants are required to complete pre- course work before attending this training. Find below links to essential trainings, please register, complete the trainings and email us certificates on or before 24 February 2020.

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 

Homepage Final EN

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

How to apply

Please email us your CV and Motivation letter to info@clinwinresearch.com and copy training-coordinator@kaviuon.org and training@clinwinresearch.com

Venue

KAVI Institute of Clinical Research, Department of Microbiology, University of Nairobi

Contacts

Tel. Mobile +254 (0)721 515 009/0790089440/722899532

Office +254 20 3673526/0703041526 /0730173526

Fax no: + 254 20 273740

Website: www.clinwinresearch.com