Key Responsibilities:


Receiving/collecting, recording of specimens;
Processing and analyses;
Preparing reagents;
Recording and reporting of results;
Dispatching the results for clinical/Research management;
Routine and daily maintenance of laboratory equipment;
Ensuring adherence to biosafety and biosecurity guidelines;
Taking part in preparation of Standards Operations Procedures (SOPs).


Vacancy Requirements:


At least eight (8) years relevant work experience    Mandatory
Diploma in Clinical Medicine;    Mandatory
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
Master’s Degree in Public health will be added advantage    Mandatory
Membership to a relevant professional body;    Mandatory
Additional training in clinical trials management/ project management related field and research ethics is an added advantage    Mandatory
Valid practicing license where applicable    Mandatory
Aleast five years’ experience working in a clinical trial or research setting will be an added advantage.    Mandatory
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
Proficiency in computer application skills.    Mandatory
Has a good understanding of role of micronutrients in human health    Mandatory
Ability to speak local dialect will be added advantage    Mandatory
Carrying out clinical trials    Mandatory
Building staff capacity through mentorship and effective leadership in the management of clinic activities    Mandatory
Communication Skills    Mandatory
Interpersonal Skills    Mandatory
Team player    Mandatory