I – Hierarchical relationship 

The Research Study Nurse will report directly to the Medical Coordinator and have a functional link with the Study Coordinator.

II – Global objective of the position 

The Research Study Nurse will ensure the integrity and quality of the research are maintained and conducted in accordance with GoT guidelines and regulations. This position is primarily responsible for the accurate recruitment and selection of study participants and collection of information as per the protocols, and for protecting the health, safety, and welfare of research participants.  

III – Tasks and responsibilities 

• Participates in recruitment and selection of study participants by interviewing and documenting medical history to determine compliance with eligibility requirements. 
• Conducts consenting process according to the principles of good clinical practice. 
• Conducts interviews and performs clinical measurements and tests according to the study SOPs 
• Administers investigational medications and performs assessments during clinic visit. 
• Records and reports adverse effects to the doctor and Principal Investigator in a timely manner 
• Accurately documents participants’ information in the study electronic database. 
• Builds a positive relationship with study participants and hospital staff 

• Follows up, in collaboration with the outreach worker, on participants for study visits. 
• Identifies study participants who defaulted and shares information with outreach worker for tracing. 
• Provides study participants with health education and medical information – to understand medication dosage, administration, disease treatment and referral to further care as needed. 
• Respects PWID and provides care in an ethical non-discriminatory manner. 
• Ensures all activities are carried out in compliance with the study protocol. 
• Participates in training and mentors the team in the research. 

IV – Requested profile  

Educational background 

• Bachelor’s degree in nursing with a valid practicing license 
• Training in Research ethics and Good Clinical Practice (GCP) 

Professional Experience  

• At least 2 years of research experience in a clinical trial or prospective cohort study 
• Experience in working with Key Populations / harm reduction programs for people who use drugs is an added advantage 
• Having (co)authored a peer-reviewed publication in the past 3 years is an added advantage 

Skills and attitude 

• Strong communication and interpersonal skills 
• Flexibility to adapt to changing requirements. 
• Ability to work with minimum supervision and handle pressure. 
• Problem solving and analytical skills. 
• Team spirit and strong motivation skills.  
• Ability to supervise, mentor and monitor the activities. 
• Precise and able to meet strict deadlines. 
• Strong reporting skills 
• Computer skills including MS Outlook, Word, Excel and Power point. 
• Fluent in both English and Swahili (reading & writing) 

How to Apply:

Please send your CV and Cover Letter to [email protected] copy to [email protected]