Clinical Research Nurse

Placements24

Bloemfontein

On-site

ZAR 320,000 - 450,000

Full time

4 days ago
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Benefits offered by this job

Medical aid
Pension fund
Professional development
Annual leave

Job summary

Placements24 is seeking a dedicated Clinical Research Nurse in Bloemfontein, SA, to coordinate and conduct clinical trials, ensuring patient safety and high-quality data collection. You will work with investigators and healthcare teams to uphold regulatory standards and ethical research conduct.

The role emphasizes venipuncture, protocol adherence, and meticulous documentation, with opportunities for professional development in a leading medical research facility.

Qualifications

  • Registered Nurse with SANC registration.
  • Minimum 3 years clinical nursing experience; 1 year in clinical research preferred.
  • Strong understanding of clinical trial phases, protocols, and regulatory requirements (GCP, ICH).
  • Excellent venipuncture and basic medical procedure skills.
  • Proficiency in data collection, documentation, and electronic data capture systems.
  • Attention to detail and organizational skills.
  • Strong communication and interpersonal skills with diverse patient populations.
  • Ability to work independently and in a team.
  • Proficiency in Microsoft Office Suite and relevant research software.
  • Commitment to ethical research conduct and patient welfare.
  • Must be authorized to work in South Africa.

Responsibilities

  • Recruit, screen, and enroll eligible participants for trials per protocol.
  • Administer study medications as prescribed.
  • Monitor health status, document vitals and adverse events.
  • Collect and document biological samples and data per protocol.
  • Educate participants about study risks/benefits and obtain informed consent.
  • Maintain accurate research records and CRFs.
  • Ensure compliance with GCP/ICH guidelines.
  • Collaborate with investigators, coordinators and sponsors.
  • Assist with physical exams, ECGs, and questionnaires.
  • Participate in site initiation, monitoring, and close-out visits.
  • Manage investigational product accountability and storage.

Skills

RN
Clinical nursing
Data capture
GCP/ICH
Venipuncture
Communication
Attention to detail
Microsoft Office
Teamwork
Ethics in research

Education

SANC registration
RN qualification

Tools

EDC systems
CRF documentation

Job description

About the Role

Our client, a leading medical research facility located in Bloemfontein, Free State, ZA , is seeking a dedicated and meticulous Clinical Research Nurse to contribute to groundbreaking medical studies. This vital role involves coordinating and conducting clinical trials, ensuring patient safety, collecting accurate data, and adhering strictly to research protocols and regulatory requirements. The successful candidate will work closely with principal investigators, study coordinators, and healthcare professionals to advance medical knowledge and improve patient care. This position offers a unique opportunity to be at the forefront of medical innovation in a supportive and professional environment in Bloemfontein . We are looking for a compassionate and detail-oriented nurse with a passion for research.

Key Responsibilities
  • Recruit, screen, and enroll eligible participants for clinical trials according to protocol requirements.
  • Administer study medications and treatments as prescribed by the principal investigator.
  • Monitor participants' health status, document vital signs, adverse events, and any changes in condition.
  • Collect, process, and meticulously document biological samples (e.g., blood, urine) and other data as required by study protocols.
  • Educate participants about the study, potential risks and benefits, and ensure informed consent is properly obtained and documented.
  • Maintain accurate and organized research records, including case report forms (CRFs) and source documents.
  • Ensure compliance with all applicable regulatory guidelines (e.g., Good Clinical Practice - GCP, ICH guidelines).
  • Collaborate effectively with the research team, principal investigators, and sponsors to ensure smooth study operations.
  • Assist with study-related procedures, such as performing physical examinations, ECGs, and administering questionnaires.
  • Participate in site initiation visits, monitoring visits, and close-out visits conducted by sponsors or regulatory agencies.
  • Manage investigational product accountability and ensure proper storage and handling of study supplies.
Requirements
  • Registered Nurse (RN) qualification with current South African Nursing Council (SANC) registration.
  • A minimum of 3 years of experience in clinical nursing, with at least 1 year in a clinical research setting preferred.
  • Strong understanding of clinical trial phases, protocols, and regulatory requirements (GCP, ICH).
  • Excellent venipuncture and basic medical procedure skills.
  • Proficiency in data collection, documentation, and electronic data capture systems.
  • Exceptional attention to detail and organizational skills.
  • Strong communication and interpersonal skills, with the ability to interact compassionately with diverse patient populations.
  • Ability to work independently and as part of a collaborative research team.
  • Proficiency in Microsoft Office Suite and relevant research software.
  • A commitment to ethical research conduct and patient welfare.
  • Must be authorized to work in South Africa.
Benefits

Our client offers a competitive salary, complemented by excellent benefits including comprehensive medical aid coverage, a pension fund, and opportunities for professional development and certification in clinical research. Employees have access to state‑of‑the‑art research facilities and a collaborative work environment dedicated to advancing medical science. This role provides a chance to contribute significantly to healthcare advancements in Bloemfontein and offers a stable career path within a reputable organization. Additional benefits include generous annual leave, paid sick leave, and potential for involvement in cutting‑edge research projects.

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