Job Description
Project description
Kenya Medical Research Institute (KEMRI) Centre for Respiratory Diseases
Research would like to fill the following vacancy in the Clinical Trials Studies to
be conducted at the KEMRI-Mtwapa Clinical Research Site in Kilifi County.
Vacancy No. CRDR/03/09/23
JOB GRADE: KMR 5
REPORTING TO: Site Investigator
Person specification:
• For appointment to this grade, a candidate must have: -
• Bachelor’s degree in Medicine and surgery from a recognized Institution;
• Registered by Kenya Medical Practitioners and Dentist Board
• Proficiency in computer application;
• At least three years’ experience working in a clinical trial or research
setting will be an added advantage
Skills and Abilities:
• Strong analytical ability, planning, and organizational skills.
• Attention to detail
• Ability to work with minimal supervision and within stipulated deadlines
and schedules.
• Excellent interpersonal and communication skills.
• Be a team player and able to work in a multi-cultural environment.
Duties and Responsibilities:
• Implementing pre-clinical and clinical research projects and/or supervise
designated aspects of the work;
• General diagnosis, care, treatment and provision of specialized clinical
care for study participants;
• Assist in carrying out fieldwork and pre-clinical and clinical experimental
procedures;
• Development of study related tools (SOPs, training materials), training of
the study staff. Medical evaluation of those participants who fulfill the
criteria for adverse events of special interest (AESI) and for reporting these
events in a timely manner.
• Medical evaluation of participants who suffer a serious adverse event and
prompt reporting as required per protocol, also on weekends and during
holidays Develop an in-depth understanding of the study design and goals
and ensure that study is conducted in compliance with study protocols
and other regulatory requirements
• Medical referral of study participants
• Handle medical emergencies at the clinical site
• Conduct Continuing Medical Education (CMEs) at the health facilities and
lead discussions with the clinical and nursing personnel. Work
harmoniously with non-study staff in the health facilities Assist with
timely and accurate data collection and data entry.
• Collaborate with the site trial manager and institution to respond to any
monitoring and audit findings and implement approved recommendations.
Perform any other duties as assigned by the site trial manager
Terms of Employment
One (1) year renewable contract as per KEMRI scheme of service with a probation
period for the first 3 months. Salary is as per the stated KEMRI scale.