Healthcare and MedicalContractorMid-level(3-5 yrs)
Job Description
Information about the role
The Study Clinical Officer will support the implementation of the Genesis project for a period of 12 months. The primary focus of this role is conducting participant recruitment, administering informed consent, and performing clinical assessments and management of STIs in accordance with Kenyan national treatment guidelines and specific study protocols. The Clinical Officer will be responsible for screening and enrolling eligible participants, performing physical and genital examinations, and collecting clinical specimens. The role requires strict adherence to Good Clinical Practice (GCP), ethical research standards, and high-quality clinical care.
Responsibilities and Duties
Participant Recruitment and Enrolment
Conduct registration, eligibility screening, and enrolment of study participants.
Provide detailed information about the study and obtain written informed consent from participants.
Clinical Assessment and Examination
Conduct comprehensive clinical assessments, including medical and sexual history for study participants.
Perform physical examinations, including genital examinations where appropriate.
Document clinical findings accurately in study case report forms (CRFs) and health facility data capture systems.
Sample Collection
Collect appropriate biological specimens according to study protocols.
Ensure proper labelling and handling of samples before transfer to the study laboratory.
Coordinate closely with laboratory staff to ensure timely testing and result reporting.
Clinical Management and Treatment
Conduct STI diagnosis and provide treatment according to Kenya national STI treatment guidelines and study protocols.
Offer counselling on STI prevention, treatment adherence, and partner notification.
Manage adverse events or complications related to study procedures.
Refer participants for additional care where necessary.
Data Documentation and Quality Assurance
Complete clinical sections of CRFs accurately and in a timely manner.
Ensure all clinical procedures follow the approved study protocol and SOPs.
Support data verification, monitoring visits, and audits.
Maintain accurate clinical records and participant files.
Collaboration and Coordination
Work closely with health facility staff, study coordinators, laboratory technologists, and data officers to ensure smooth implementation of study activities.
Participate in study meetings, trainings, and protocol review sessions.
Provide technical input during monitoring visits and reporting processes.
Prepare weekly and monthly reports on the study progress.
Ethical and Regulatory Compliance
Ensure adherence to Good Clinical Practice (GCP), national STI management guidelines, and ethical requirements.
Maintain participant confidentiality and ensure ethical conduct throughout the study.
Report adverse events and protocol deviations as required.
Skills, Experience, and Qualifications
Registered with the Clinical Officers Council (COC) of Kenya with a valid practicing license.
At least 2–3 years of clinical experience, preferably in sexual and reproductive health or STI/HIV services.
Experience working in clinical research or public health programs is an added advantage.
Training in Good Clinical Practice (GCP) is desirable.
How to Apply
Interested and qualified candidates should apply online via the International Centre for Reproductive Health careers portal at careers.icrhk.org.
How to Apply
Interested and qualified candidates should apply online via the International Centre for Reproductive Health (ICRH) Kenya application portal at https://careers.icrhk.org. Alternatively, visit the application link here.
