Research Nurse

SUMMARY:
If you’re passionate about patient care, clinical research, and making a meaningful impact in community health, this role offers an exciting opportunity to work within a fast-paced and purpose-driven research environment.
 
The University of Cape Town Lung Institute is looking for a professional and compassionate Research Nurse to support the implementation and coordination of clinical research studies through participant care, clinical procedures, protocol-related activities, and accurate study documentation in accordance with Good Clinical Practice (GCP) standards.
 
This role is offered under the University of Cape Town Lung Institute’s own employment terms and conditions, which are separate from UCT conditions of service.

POSITION INFO:
🩺 What you bring:

• Degree / Diploma in General Nursing
• Minimum 2 years’ general nursing experience (post community service)
• Clinical assessment, phlebotomy, and vaccination experience
• Good Clinical Practice (GCP) Certification advantageous
• Fluency in English and a second language (Afrikaans and/or isiXhosa)
• Excellent interpersonal, communication, organisational, and time management skills
• Ability to work independently and within a multidisciplinary Research team

• Conduct informed consent and perform protocol-required clinical procedures in line with study requirements
• Provide pregnancy and contraception assessment and counselling, HIV pre- and post-test counselling, risk-reduction guidance, and adherence support
• Perform clinical assessments including vital signs, symptom review, specimen collection (urine, blood, vaginal swabs), and administration and monitoring of study drugs/vaccinations
• Conduct point-of-care testing including pregnancy tests, urinalysis, HIV, haemoglobin, and glucose testing
• Collaborate with laboratory staff regarding sample processing and storage according to protocol requirements
• Ensure accurate data documentation in compliance with GCP standards and assist with data entry and query resolution
• Perform quality control checks on participant files in accordance with SOPs
• Support study and site administration including stock control, ordering of consumables and laboratory kits, infection control, and biohazard waste management
• Maintain fully stocked clinic rooms and emergency trolley readiness
• Assist with clinic bookings and participant flow to ensure efficient site operations
• Attend meetings and required training sessions and maintain access to study management systems
• Communicate effectively with internal and external stakeholders across multiple platforms

• Fixed Term Contract (12 Months)
• Monday to Friday | 40 hours per week
• Based in Khayelitsha