Research Nurse Task Clinical Research Centre

**About the Company**:
TASK is a South African headquartered, multinational clinical research institute that conducts clinical trials to determine the treatment effects of novel medicinal products or devices in healthcare and offers services in conducting complex clinical trials in a wide variety of therapeutic areas.

**Overall Purpose of the Position**:
The purpose of this role is to perform procedures following the visit schedule as stipulated in each protocol and monitor the health and safety of the participants, and document the response to an intervention, which is typically new drug or therapy in the source documents. The Research Nurse (RN) ensures that the clinical trials are always run according to protocol requirements ensuring all procedures are documented in source and data is accurately transcribed onto clinical research forms (CRF) or electronic-CRF’s.

**Key Performance Areas (KPAs) & Responsibilities include, but not limited to**:

- Familiarizing themselves with study specific protocols and requirements and stay up to date with amendments.
- Undertaking the informed consent (IC) process by presenting a study to possible participants and/or family members.
- Assisting the investigator in ICF signing process and ensure that adequate time and privacy for reflection and answering questions has been provided. Performing quality checks on ICF (informed consent form).
- Performing the quality checks and completion of study documentation, including source, case report forms (eCRFs) and study logs.
- Educating participants on study related requirements and compliance.
- Planning visit study specific procedures ahead and performing procedures in accordance with protocol requirements following prompts and flow of the relevant source documents; Documenting participant feedback, investigator product compliance and related care and procedures in source documents.
- Familiarizing themselves with normal ranges in vital signs, ECG measurements, and safety blood ranges, to identify abnormalities and act/document accordingly to ensure participant safety.
- Familiarising themselves with special study specific safety reporting requirements.
- Collecting biological specimens (sputum, saliva, blood, etc.), preparing specimens where needed and completing any related documents, logs and checklists accurately and in real time according to GCP specifications.
- Administering Investigational Product (IP) as per protocol and keeping the IP administration log up to date and verifying storage are within allowed range as per protocol.
- Providing the clinical and administrative nursing support and oversight whilst creating a safe and participant friendly environment during clinical study conduct.
- Performing miscellaneous job-related duties as assigned.
- Competent in nursing procedures according to registration scope of practice and including, but not limited to, monitoring and recording of vital signs, general wellbeing, ECG measurements, performing phlebotomy, IV preparation, administration and monitoring, medication administration and control as well as resuscitation procedures.

**Ideal Requirements**
- Nursing diploma or degree (Registered nurse) or a qualified Enrolled Nurse.
- Valid Nursing Council certificate (SANC).
- Valid ICH GCP certificate.
- Strong administrative skills.
- Computer and internet competency and basic knowledge of Microsoft Word, Excel, Outlook.
- Practical experience in research and/or clinical trials would take preference.
- Valid Driver’s License
- Flexibility to work at other TASK sites and to accommodate occasional night and weekend schedules.

**Key Personal Inherent Characteristics**
- Communicating effectively in English (verbal and written).
- Excellent inter-personal skills.
- Good team player, has diplomacy and tact.
- High attention to detail.
- Excellent follow up skills.
- Friendly.
- Planning and working in an organised manner.
- Efficient.

**Details**:
**Area**:Bellville, Cape Town

**Contract Type**:12 Months Fixed Term

**Applications Close**:10 December 2024

TASK reserves the right to withdraw this advertisement and not fill the above-mentioned vacancy at any stage during the recruitment process.

Meeting our employment equity goals will be acknowledged during the recruitment process.

**Job Types**: Full-time, Temporary
Contract length: 12 months

Application Question(s):

- What is your notice period?
- What are your gross salary expectations?

Application Deadline: 2024/12/10