KEMRI/UW Study Coordinator Job in Kisumu Kenya

The Kenya Medical Research Institute (KEMRI) in collaboration with the University of Washington (UW) is conducting research studies at multiple sites in Kenya including Kisumu, Kisii and Nairobi.

The KEMRI/UW study project seeks to recruit a dynamic experienced individual to fill the following position:

Study Coordinator Kisumu Site

The Study Coordinator will be responsible for the coordination of clinical trials and observational studies.

S/he will manage the project on a day-to day basis, recruit research participants and oversee the collection of study and trial data whilst ensuring that these research processes adhere to regulatory requirements.

Qualification

 

• Registered Nurse or higher diploma with at least three years of study coordination experience in a clinical research setting.
• Master’s Degree in Public Health would be an added advantage
• Be able to write manuscripts and publications
• Be able to design, amend and implement HIV Research Protocols
• Be able to develop case report forms and assist with primary analysis as per the study objectives
• Be able to give technical advice to both his/her supervisee/supervisor
• Be able to manage and supervise study staff
• Computer literate (Word, Excel)
• Good communication and organizational skills
• More than 3 years experience in Clinical Research
• Be able to work in fast paced environments
• Be a team player
• Willing and ready to travel within country

Responsibilities

• The clinical study coordinator will act as point person for the Study.
• Will perform all human-resources duties including recruitment and terminations.
• 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.
• Recruits and enrolls participants into the study.
• Maintains strong relationship with study clinical sites and community groups involved
• Prepares and prints all reports related to the study as requested by the study investigators.
• Develop standard operating procedures and best practices for the study
• Ensure that study enrollment is occurring smoothly
• Ensure that all patients are receiving adequate information prior to consent and that all data forms are filled out appropriately
• Ensure that participant charts and specimens are conveyed daily between clinic site and the laboratory
• Coordinate staff evaluation procedures
• Make monthly reports on the administration of the study
• Sees to it that all remain in compliance with local, state and federal regulations.
• Should uphold the mission and vision of KEMRI/UW Organization
• Perform other duties that may be given by the Investigators

Terms of Employment:

One year renewable contract as per KEMRI scheme of service and a probation period for the first 3 months. The successful candidate shall be based in Kisumu.

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://spreadsheets.google.com/spreadsheet/viewform?formkey=dFVxRXR0OWVHY0F6X1lHaTZiTm9RNGc6MQ
and 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 25th August, 2011 at 5.00 p.m.

Note: Only the shortlisted candidates will be contacted.

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