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Enrolled Research Nurse

University of Cape Town

Cape Town

On-site

ZAR 300,000 - 400,000

Full time

3 days ago
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Job summary

A leading university in South Africa is seeking an Enrolled Nurse to support clinical research projects. The ideal candidate will have a Certificate in Enrolled Nursing, 3 to 5 years of clinical research experience, and fluency in English. Responsibilities include participant recruitment and clinical administration. This role offers opportunities to contribute to important health research.

Qualifications

  • 3 to 5 years’ experience in clinical research.
  • Ability to work under pressure.
  • Credit and criminal records clear.

Responsibilities

  • Recruit eligible participants for research projects.
  • Screen participants using specified criteria.
  • Administer medications as per study protocol.

Skills

Certificate in Enrolled Nursing
Clinical research experience
Fluency in English
Interpersonal skills
Communication skills
Time management
MS Office proficiency
Phlebotomy skills
Organizational skills
Teamwork

Education

Certificate in Enrolled Nursing

Tools

Data Management Systems

Job description

Job Location : Western Cape, Cape Town Deadline : August 21, 2025 Quick Recommended Links

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Essential Requirements :

  • Certificate in Enrolled Nursing and current registration with the South African Nursing Council (SANC) as an Enrolled Nurse
  • 3 to 5 years’ experience in Clinical research on Multiple projects
  • Fluency in English, Afrikaans and / or isiXhosa
  • Excellent interpersonal, communication (both verbal and written) and time management skills.
  • Proficiency in MS Office (Word, Excel, PowerPoint, and Internet)
  • Excellent phlebotomy skills
  • Strong organizational skills
  • Detail-orientated
  • Proactive and self-motivated
  • Ability to work under pressure and in a fast-paced environment
  • Ability to maintain the integrity of research studies.
  • Open-minded and always willing to learn
  • Flexible; able and willing to make changes to work schedule to meet the demands of the company
  • Willingness to travel to various CLII research sites within Cape Town
  • Ability to work in a team and independently and to foster a collaborative relationship with local clinics and hospitals
  • Credit and Criminal Clear

The following will be advantageous :

  • Interest in Infectious Diseases Research
  • Knowledge of Good Clinical Practice (GCP) with current GCP certification
  • Previous experience working with TB patients, especially drug-resistant TB patients.
  • Valid Driver’s license (advantageous) and own reliable transport
  • Proficiency in Data Management systems

Responsibilities include (but not limited to) :

Participant recruitment, enrolment and retention :

  • Recruitment of eligible participants for research projects(s)
  • Administration of informed consent and all study related activities
  • Providing support and education to participants regarding the study
  • Assist the coordinator to monitor trial related activities, i.e. enrolment, recruitment and randomization processes
  • Ensure relevant data is collected from source documentation i.e. copies of Identity documents, birth certificates etc.

Clinical :

  • Screen participants for inclusion into the study using specified inclusion and exclusion criteria
  • Scheduling of participants for clinical examination and follow up
  • Arrange participant transport and arrange and book participants follow up visits and telephone calls.
  • Ensure that the necessary documents are available and ready for each study visit.
  • Ensure that results are received and seen by the Investigators and ensure that abnormal results are followed up as requested.
  • Monitoring trial related activities, before, during and after the trial
  • Obtain participant specimen samples i.e. perform phlebotomy, collecting urine and saliva
  • Completing Point of care test i.e. Rapid test for Pregnancy, Retroviral status, other
  • Coordinate transportation of biomedical samples to the relevant laboratories
  • Complete laboratory specimen transfer / transport logs.
  • Administering medications or treatments as per the study protocol and under supervision of the Registered Nurse

Study Administration, Collection and Management :

  • Maintain record of all communications as required.
  • Ensure all study procedures and tests are properly documented in source according to ICH GCP guidelines.
  • Assist with participant record management
  • Collecting and documenting data on case report forms (CRFs).
  • After trial ensure all data collected and filed away in correct order
  • Entering data into electronic databases
  • Performing quality control checks on data to ensure accuracy.
  • Assist Coordinator with administrative duties relating to regulatory functions
  • Maintain accurate records for inventory of clinical stock, equipment, material and supplies

Ad-hoc Duties

  • Assist with participant reimbursement and petty cash management i.e. submission of receipts, collecting of petty cash etc.
  • Assist with archiving and any other research-related duties as required
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