Key Responsibilities:
Participate in participant review and care, and all
study procedures as guided by study protocols.
Perform pelvic exams, cervical cancer screening,
contraceptive counselling administration, and removals
Perform phlebotomy on all study participants
Assess adherence to study products and take
anthropometric measurements
Prepare weekly and monthly progress reports of study
activities
Monitor adverse events and report them to the safety
monitor as required.
Act as liaison between investigators, and
participants.
Promote good clinical practice in the conduct of
clinical studies and provide medical input at all stages of the project
lifecycle
Perform any other job-related duties as may be
requested or required
Vacancy Requirements:
Bcahelor’s Degree in Medicine and Surgery
(MBChB Mandatory
A valid retention certificate from KMPDC
Mandatory
Demonstrated competence in female reproductive health
service delivery, including cervical cancer screening, counseling, and
provision of various contraception methods Mandatory
Two years’ experience in a similar field.
Mandatory
Experience in a research setting and having a Human
Subject protection certificate will be an added advantage
Added Advantage
Excellent interpersonal skills to deal effectively
with clinicians, other study staff, participants, administrators, regulators,
monitors, and sponsors. Mandatory
Familiarity with the Microsoft Office
Suite. Mandatory
Excellent organizational skills to independently
manage workflow. Mandatory
Ability to prioritize quickly and
appropriately Mandatory
Ability to multi-task. Mandatory
Meticulous attention to detail
Mandatory
Excellent written and verbal communication skills
How To Apply
