About

I am a Research Pharmacist with more than 7 years progressive experience in the conduct of clinical trials. I am trained in pharmacy, medicinal chemistry, and clinical research. As a member of the senior clinical management team I participate in strategic and operational decision making involving clinical trial selection, protocol development, institution review boards (IRBs) submission, protocol planning and progress review, monitoring and close out activities. I am also a reviewer with the Kenya Medical Research Institute (KEMRI) center for clinical research where I review protocols and other clinical trial related documents. My key competencies include investigational products supply chain management, implementation of International Conference on Harmonization (ICH), Good clinical practices (GCP) and Human Subject Protection (HSP) guidelines, regulations and policies, formulation and implementation of general and study specific procedures (SOPs), pharmacy quality control/quality assurance plans and pharmacy establishment plans in line with local and international regulatory requirements. As Pharmacist of Record (POR), I organize, facilitate and train clinic research staff on all general and protocol-specific procedures, and handle the day-to-day pharmacy operations. I am also the liaison officer between National Institute of Health (NIH) Division of AIDS (DAIDS) Pharmaceutical Affairs Branch (PAB) and the site on all issues regarding IP management.

Skills

  • Strategic Planning
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Experience

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Research Pharmacist

  • Kenya, Nairobi
I am a Research Pharmacist with more than 7 years progressive experience in the conduct of clinical trials. I am trained in pharmacy, medicinal chemistry, and clinical research.
As a member of the senior clinical management team I participate in strategic and operational decision making involving clinical trial selection, protocol development, institution review boards (IRBs) submission, protocol... planning and progress review, monitoring and close out activities. I am also a reviewer with the Kenya Medical Research Institute (KEMRI) center for clinical research where I review protocols and other clinical trial related documents.
My key competencies include investigational products supply chain management, implementation of International Conference on Harmonization (ICH), Good clinical practices (GCP) and Human Subject Protection (HSP) guidelines, regulations and policies, formulation and implementation of general and study specific procedures (SOPs), pharmacy quality control/quality assurance plans and pharmacy establishment plans in line with local and international regulatory requirements.
As Pharmacist of Record (POR), I organize, facilitate and train clinic research staff on all general and protocol-specific procedures, and handle the day-to-day pharmacy operations. I am also the liaison officer between National Institute of Health (NIH) Division of AIDS (DAIDS) Pharmaceutical Affairs Branch (PAB) and the site on all issues regarding IP management.
 more
  • Strategic Planning
  • Pharmacist of Record at   Usamru-k.org  
  • September, 2015 -