Research Nurse Co-ordinator

2 weeks ago


Durban, South Africa University of KwaZulu-Natal Full time

**The University of KwaZulu-Natal (UKZN) is committed to meeting the objectives of**

**Employment Equity to improve representativity within the Institution. Preference will be**

**given to applicants from designated groups in accordance with our Employment**

**Equity plan.**

**COLLEGE OF HEALTH SCIENCES**

**RESEARCH NURSE CORDINATOR**

**(6 Months Fixed-Term appointment) Internal Medicine**

**SCHOOL OF CLINICAL MEDICINE**

**MEDICAL SCHOOL CAMPUS**

**REF NO.: T/CM11/2023**

The Division of Internal Medicine is seeking a dynamic and experienced

Professional Nurse to fill the position of Research Nurse and Study Coordinator for

the WHO - RANDOMISED EVALUATION OF COVID-19 THERAPY (RECOVERY) project for

the South African eThekwini site and other related research activities. The

of the RECOVERY study and the day-to-day running of the study in all

selected sites under the leadership of Professor N Magula and Professor S Pillay

(University of KwaZulu-Natal). S/he will be required to engage the principal

investigators and their team at the University of KwaZulu-Natal, other co
- investigators, the study doctor, pharmacist, and administrative officers at all

project sites, the Finance Officer of the College of Health Sciences, research

assistants, and administrative officers at all project sites. S/he may be required to

perform additional roles as determined by the Principal Investigator.

**Minimum Requirements**:

- Matric
- Current registration as a professional nurse with the South African Nursing

Council (SANC)
- 10 years or more experience as a Professional nurse.
- More than 1year experience in conducting randomized controlled Covid-19

global clinical trials.
- Experience in the South African Products Authority Process
- Valid Good Clinical Practice Certificate process
- Valid Driver’s license and own transport
- Manage the RECOVERY project and ensure that pre-established work scope,

Inspection visits for Covid-19 clinical trials study protocol and regulatory

requirements are followed.
- Recruit and train research assistants as appropriate and serve as principal

administrative liaison for the project.
- Recruit, enroll and follow up research participants.
- Administer telephonic and online questionnaires.
- Manage site inspection visits by the South African Health Products Regulatory

Authority (SAPHRA).

**Essential requirements**:

- Strong knowledge of research administration including quality assurance and

research ethics
- Advanced MS Office skills
- Experience with electronic databases (collation, data entry and data

analysis) and basic statistical analysis
- Experience in financial management
- Excellent planning, coordinating and problem-solving skills
- Excellent written and oral communication skills
- Valid motor vehicle driver's license and own transport
- Experience in working with a multidisciplinary team
- Past experience with regulatory matters
- Experience with community based clinical research
- Knowledge of UKZN policies and processes

This post reports to t h e Principal Investigators. The job profile is available from

**right not to make any appointment.**

**the position. Please provide three names of referees, including their contact details.


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