KEMRI Study Clinician Jobs in Kenya

KEMRI Study Clinician Jobs in Kenya

Reports to: Study Coordinator

Location: Kisumu

Duration: 6 Months as per KEMRI Scheme of Service. The first 2 months is a probation period

Duties and Responsibilities:

• Register and consent study participants and assist with eligibility determination, screening and enrolment of study participants.

• Administer and collect participant tobacco use history and medication use history as per study
protocol.

• Provide health education on tobacco use cessation counselling support.

• Screening and enrolment of participants.

• Administer study intervention medication

• Monitor and report AEs

• Respond to questions about the study posed by participants and the community.

• Ensure participant retention and adhere to site retention strategies and requirements.

• Maintain up to date participant visit notes.

• Administer Case Report Forms (CRFs), accurate recording of data on CRFs and perform self QC.

• Assess adherence to study products.

• Develop and review study related SOPs.

• Laboratory results interpretation.

• Prepare weekly and monthly progress reports of personal study activities.

• Closely work with other staff members to ensure the success of the study.

Qualifications

• Diploma in Clinical Medicine and hands-on Clinical experience.

• Must be registered with the Clinical Officers Council of Kenya.

Required Experience

• At least 2 years of clinical experience working in a busy HIV clinic.

• Good Clinical Practice training/Human Subjects Protection training in behavioural Health

• More than two (2) years Clinical research experience is an added advantage.

• Knowledge of tobacco cessation interventions will be an added advantage


How to Apply

For more information and job application details, see; KEMRI Study Clinician Jobs in Kenya

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