The Kenya Medical Research Institute (KEMRI) in collaboration
with the University of Washington (UW) and University of Nairobi (UoN) are in
the process of conducting a research project evaluating PMTCT services at
multiple sites in Kenya.
The KEMRI / UW / UoN study project therefore seeks to recruit dynamic,
innovative and experienced person to fill the following position: Study Coordinator
The Study Coordinator will be responsible for the coordination
of all project activities to ensure smooth implementation of the study.
She/he will manage the project on a day-to day basis, including
preparation of SOPs, recruitment and training of other study staff, coordinate
field work activities including procurement and distribution of supplies and
oversee the collection of study data whilst ensuring that these research
processes adhere to regulatory requirements.
The study coordinator will generate regular reports on the progress
of the study, give technical advice to both his/her supervisee/supervisor and
should be able to manage and supervise study staff.
He or she should be able to work in fast paced environments with
minimal supervision and be a team player.
Qualification
Qualification
- Registered
Nurse/Higher Diploma in nursing/Degree in Nursing or equivalent relevant
qualification with at least two or more years of study coordination
experience in a clinical research setting. (Master’s Degree in Public
Health would be an added advantage)
- Have
background experience with PMTCT activities.
- Computer
literate (Word, Excel).
- Good
communication and organizational skills.
Responsibilities
- The
study coordinator will act as point person for the Study.
- Will
perform all human-resources duties including coordinating recruitment,
training and supervision of the other staff.
- Scheduling
and managing all staff members at various study sites, training new staff
members including giving briefings on all operational policies and
procedures; ensuring each person understands his/her role and
responsibilities.
- Maintain
strong relationship with study clinical sites and stakeholders involved in
the study
- Prepare,
print and distribute all reports related to the study that study
investigators request.
- Develop
standard operating procedures and best practices for the study
- Ensure
smooth and efficient study enrollment.
- Ensure
that participant charts and specimens are conveyed daily between clinic
site, laboratory and the Data office.
- Make
monthly reports on the administration of the study.
- Perform
other duties that may be given by the Investigators.
- Ensure
that there is compliance with local, state and federal regulations.
Terms of Employment:
The successful candidate will be given initially a 6 months
contract as per KEMRI scheme of service and a probation period for the first 3
months.
This may be considered for extension depending on the dates of
start and closure of fieldwork.
The successful candidate shall be based in Nairobi
Remuneration:
Remuneration:
Compensation is negotiable within a relevant grade, based on
educational levels, relevant experience and demonstrated competency.
The salary scheme is based on the KEMRI salary scales.
If you meet the above requirements, please follow the following
link to complete the application form:https://docs.google.com/spreadsheet/viewform?formkey=dDBoSlN2dzd1M3FjNk5TQkc5QkhEZGc6MQ and then send an application letter with your current CV that
contains details of your qualifications, experience and the full time telephone
number and names and addresses of 3 professional referees and copies of
certificates and testimonials to Email address: kemriuwjobs@gmail.com to reach
us by Thursday, 9th August 2012 at 5.00 p.m.
Note: Only the shortlisted candidates will be contacted.
Note: Only the shortlisted candidates will be contacted.
All those invited for interviews will be expected to have GCP
Certificate as well as Human Subject Protection training.