Kenya Medical Research Study Coordinator - Bungoma Jobs in Kenya
Key Responsibilities:Identifying research gaps in line with the Institute’s research priority areas;
Development of research proposals in the relevant research thematic area;
Implementing pre-clinical and clinical research projects and/or supervise designated aspects of the work;
Conducting medical examinations and writing medical reports;
General diagnosis, care, treatment and provision of specialized clinical care for study participants;
Conducting community diagnosis, care and treatment during Corporate Social Responsibility (CSR)
activities;
Establishing strategic partnerships for research, training, innovations, technology;
Sourcing for grants to fund the approved research protocols;
Supervising junior professional and technical staff attached to his/her pre-clinical and clinical research program
Monitoring and evaluating implementation of research projects;
Writing manuscripts, reports and translating research findings into lay language;
Disseminating and translating research findings for evidence based policy formulations and implementation;
Identifying technology with potential for intellectual property protection;
Vacancy Requirements 1 At least eight (8) years relevant work experience Mandatory
2 Diploma in Clinical Medicine; Mandatory
3 Higher Diploma in Clinical Medicine such as Anaesthesia, Oral Health, ENT, Pediatrics, Lung/Skin, Orthopedics, Reproductive Health, Epidemiology, dermatoenerology, Ophthalmology and Cataract Surgery from a recognized institution; Mandatory
4 Master’s Degree in Public health will be added advantage Mandatory
5 Membership to a relevant professional body; Mandatory
6 Additional training in clinical trials management/ project management related field and research ethics is an
added advantage Mandatory
7 Valid practicing license where applicable Mandatory
8 Aleast five years’ experience working in a clinical trial or research setting will be an added advantage. Mandatory
9 Certificate in “Good Clinical Practice”, “Human Subjects Protection” and ICH training skill; and Good understanding of Good Clinical Practice (GCP) guidelines and clinical trial regulations Mandatory
10 Proficiency in computer application skills. Mandatory
11 Has a good understanding of role of micronutrients in human health Mandatory
12 Ability to speak local dialect will be added advantage Mandatory
13 Carrying out clinical trials Mandatory
14 Building staff capacity through mentorship and effective leadership in the management of clinic activities Mandatory
15 Communication Skills Mandatory
16 Interpersonal Skills Mandatory
17 Team player Mandatory
How to ApplyFor more information and job application details, see;
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