Key Responsibilities:
Oversee all clinic and other study personnel
performing study specific tasks and procedures.
Monitors adverse events and reports them to the
safety monitor as required.
Act as liaison between investigators, participants
and staff.
Ensure preparedness of staff and site for study
implementation.
Provide training, mentorship to clinical team in all
aspects of trial conduct and project orientation to ensure compliance with
protocols and guidance documents
Promote good clinical practice in the conduct of
clinical studies and provide medical input at all stages of the project
lifecycle
Participate in participant review and care, and in
all study procedures as guided by study protocols.
Oversee regulatory submissions and approvals to local ethical review committees and liaise with other project managers to ensure timely submissions to international institutional review boards.
Maintain all study records including but not limited
to, regulatory binders, study specific source documentation and other materials
as required.
Coordinates and facilitates monitoring and auditing
visits, notifies appropriate institutional officials audits, responses to any
findings and implements approved recommendations.
May perform other job-related duties as requested or
required
Vacancy Requirements:
Degree in Medicine and Surgery (MBChB)
At least 3-year work experience as a medical officer
Experience and competence in providing HIV care
clinical care services
Previous management and leadership
experience Added Advantage
Experience providing reproductive health
services. Added Advantage
Knowledge of clinical trial ethics and Good Clinical
Trial Practice Added Advantage
Must have valid retention certificate from KMPDC
Excellent interpersonal skills.
Familiarity with the Microsoft Office Suite.
Excellent organizational skills to independently
manage work flow.
Ability to prioritize quickly and appropriately
Ability to multi-task.
Meticulous attention to detail
How To Apply
