Key Responsibilities:
Performing Clinical Assessments.
Collecting specimens.
Conducting interviews, administering Case report
forms, and form completion
Offer support counseling to study participants.
Conducting the informed consent process.
Diagnose and provide STI and treatment for other
ailments to participants.
Make requisitions for the required clinical supplies.
Monitor Adverse events and write reports to IRB or
any other regulatory body as required
Develop and implement Standard Operating Procedures
as per protocol
Perform any other duties as assigned by immediate
supervisor.
Safety communication with the medical director, study
safety monitor, and Principal Investigator
Vacancy Requirements:
Diploma in Clinical Medicine
Valid practicing license.
At least two (2) years Clinical research
experience
Demonstrated competence in female reproductive health
service delivery, including cervical cancer screening, counseling, and
provision of various contraception methods
Knowledge of HIV prevention and treatment
services
Good Clinical Practice training/Human Subjects
Protection training in mental Health/Psychiatry Nursing, is an added
advantage Added Advantage
Commitment to integrity and high-quality
performance
Good interpersonal skills and ability to work in a
team
Keen and attentive to detail
Ability to follow instructions and
procedures
Articulate in both verbal and written communication
in English and Swahili
Counselling skills Added
Advantage
Computer literacy
How To Apply
