Benard Kipsang
Clinical Research Coordinator
I am highly motivated, organized scientist and cancer advocate seeking to work in a research setting with the goal of providing research service utilizing my extensive skills and experience in primary healthcare background.
Work Experience
- 2003 - 2023Henry Jackson Foundation Medical Research International - Kemri/Walter Reed ProjectClinical Research Coordinator• Mobilization, Assessment and selection of potential study volunteers;
• briefing, informed consent education and administration;
• scheduling of appointment;
• medical history & physical examination;
• assessing vital signs, treatment of volunteers, management and reporting of adverse events;
• filling of source documentation; completion, review and correction of Case Report Forms (CRF),
• Protocol development,
• prepare documents for submission to the IRBs and other regulatory authorities,
• ensure adherence to protocol by all and compliance with applicable laws, regulations policies and procedural requirements,
• oversee and coordinate recruitment, care and treatment of research subjects and liaise with other internal departments and external collaborators,
• oversee study- related activities such as chart preparation, protocol trainings, SOP development, preparation of relevant study forms and labels,
• Volunteer selection, recruitment and enrollment, administration of consent forms,
• planning, scheduling and carrying out of procedures to provide adequate care and treatment of research subjects.
• Contact volunteers and schedule follow up appointments as appropriate.
• Perform interval interviews and assessments at study visits for protocol specific data.
• Enter data for specific visit on CRF; audit records for accuracy, and ensure completed CRFs in a timely manner.
• Resolve data and record discrepancies identified during the in- house reviews.
• Schedule monitoring and Coordinate staff in preparation for monitoring visits.
• Perform periodic review of the regulatory binder to ensure completeness.
• Prepare protocol required reports such as SAEs, Continuing Review Reports and other reports as may be necessary.
- 2003 - 2003Litein HospitalClinical Officer• Medical history, physical examination, assessment of vital signs,
• treatment and referral of patients for specialized treatment;
• Diabetic clinic management;
- 2000 - 2003Tenwek HospitalClinical OfficerResponsibilities:
• Medical History, Physical Examination, treatment and referral of patients for specialized treatment;
• Medical and Diabetic Clinics Management;
• Supervision and Clinical instruction for student nurses, Medical Officers interns and clinical officers' interns;
• duty assignment for other clinical officers,
• coordinating Continuous Medical Education (CME),
• assistant in-charge clinical officer.
Education
- 2021 -University of ManchesterOngoing Master's Degree
- 2018 - 2021University of KabiangaBachelor of Science Clinical Medicine
- 1997 - 2000Kenya Medical Training CollegeDiploma in Clinical Medicine
- 1992 - 1995Tengecha High SchoolKenya Certificate of Secondary Education
Hobbies
- • Excellent written and verbal communication skills
- • Knowledge of FDA and ICH guidelines
- • Study design and protocol development
- • Study subject’s recruitment
- • Data collection and analysis
- • Project management
- • Problem-solving
- • Ethical considerations
Personal Details
- Sex: Male
- Marital Status: Married
- Religion: Christian
- Nationality: Kenyan
- Date of Birth: 29/03/1977
References
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