Brian Kabuubi Email & Phone Number | A Clinical Research Professional with more than 10 years of working experience in Clinical Research and Quality Management. I worked as a clinical trial medical technologist, then as an Investigative site quality manager and currently as a Clinical Research Associate. I have been involved in infectious diseases including HIV and Malaria in Uganda, Kenya, Tanzania, Malawi, Mozambique, SouthAfrica and Sudan. I have performed study start-up activities, site audits, initiation, monitoring, and general site management with both naïve and experienced sites. Strong skills in; • ICH GCP and FDA regulations • Div. V of Canada F&DA, SSU, Clinical Trial Conduct & Monitoring • Site Evaluation, Selection and Initiation. • Data collection/Data Management, Query Resolution, and Close-out. CTMS-Impact EDC-Medidata Rave RBM platform- CluePoints Microsoft office

Brian Kabuubi

A Clinical Research Professional with more than 10 years of working experience in Clinical Research...
Uganda

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Brian Kabuubi’s Email brian.kabuubi@iqvia.com

Brian Kabuubi’s Phone Numbers

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Brian Kabuubi’s Location Uganda

Brian Kabuubi’s Current Industry

Brian Kabuubi’s Prior Industry Pharmalys | Uvri Iavi Hiv Vaccine Program | Cra School Of Montreal | Mildmay

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Senior Clinical Research Associate

Present

Clinical Research Associate

2018-04-01 00:00:00 - 2020-12-01 00:00:00

Qa Manager

2015-01-01 00:00:00 - 2018-04-01 00:00:00

Clinical Research Intern

2017-02-01 00:00:00 - 2018-04-01 00:00:00

Medical Technologist

2006-01-01 00:00:00 - 2007-07-01 00:00:00

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Brian Kabuubi is a A Clinical Research Professional with more than 10 years of working experience in Clinical Research and Quality Management. I worked as a clinical trial medical technologist, then as an Investigative site quality manager and currently as a Clinical Research Associate. I have been involved in infectious diseases including HIV and Malaria in Uganda, Kenya, Tanzania, Malawi, Mozambique, SouthAfrica and Sudan. I have performed study start-up activities, site audits, initiation, monitoring, and general site management with both naïve and experienced sites. Strong skills in; • ICH GCP and FDA regulations • Div. V of Canada F&DA, SSU, Clinical Trial Conduct & Monitoring • Site Evaluation, Selection and Initiation. • Data collection/Data Management, Query Resolution, and Close-out. CTMS-Impact EDC-Medidata Rave RBM platform- CluePoints Microsoft office