Job Description
KEMRI–CCR PHRD (Thika) clinical trials Project is currently looking for a motivated
individual to fill in the following vacant position:
Position: Study Administrator KMR 6 (1 position)
Location: Thika
Reports to: Principal Investigator
Job purpose:
To offer project administrative support at the PHRD Thika Clinical Research site.
Responsibilities:
- Participate in regular study calls
- Assist in making calls to principal investigators
- Assist in keeping track of study activities against target milestones
- Assist the Principal Investigators in preparing study implementation reports.
- Assist the Principal Investigators in their day-to-day study implementation activities
- Assist in filling study questionaries and forms
- Assist in drafting and distributing study letters
- Maintain and keep track of study calendar
- Provide logistical support for workshops and project meetings
- Perform clerical duties including photocopying, scanning, filing, and mailing
- Assist in regulatory submissions.
STAFF QUALIFICATION AND COMPETENCIES
Education and Professional training
- Bachelor’s Degree in Business Administration, Monitoring and Evaluation or any
related field
Competencies
- Excellent communications skills
- Team Player
- Excellent computer skills
- Excellent report writing skills
- Mature and self-motivated
- High Integrity and confidentiality
- Good planning and organizing skills
- Ability to work independently
Experience
- At least two (2) years of experience.
Terms of employment
Employment is a six months contract with a probation period for the first 2 months. Salary
is negotiable within the appropriate grade depending on education, experience and
demonstrated competency