Africa Clinical Research Network (ACRN) is an African-led clinical research organization building the next generation of trial capacity across the continent. We work with existing hospitals, research units, and investigators to enable high-quality clinical research—from investigator-initiated studies to late-phase and registration trials—while strengthening local systems, skills, and infrastructure.
ACRN operates as a pan-African site management and research delivery platform, combining strong clinical operations, regulatory expertise, data and digital systems, and quality management. Our model is practical and embedded: we focus on making trials work in real settings, reducing friction for sites, sponsors, and regulators, and delivering reliable, audit-ready data.
We partner closely with governments, regulators, academic institutions, and industry to expand Africa’s role in global clinical research, while ensuring that studies generate local value—through workforce development, institutional strengthening, and improved patient care.
At ACRN, you’ll work on meaningful, complex projects with global impact, alongside a multidisciplinary team that values rigor, accountability, and innovation. We are building something durable, ambitious, and distinctly African—and we are looking for people who want to help shape it.
About the Opportunity
Are you a newly qualified nurse who has just completed your internship? Curious about research and looking for a unique career path beyond traditional nursing?
This is your chance to step into the world of clinical research. No prior research experience is needed. We are looking for passionate, motivated nurses ready to learn, grow, and gain hands-on experience in a dynamic research environment.
This is an entry-level clinical research support role, operating under supervision within a regulated ICH-GCP environment.
What you’ll do
- Participant Care
- Provide safe, respectful nursing care and monitor participant health during study visits.
- Study Support
- Assist with scheduling, participant visits, and basic study coordination activities.
- Clinical Procedures
- Support sample collection (e.g., blood, urine) and perform basic clinical assessments (vitals, observations).
- Safety Monitoring
- Observe and report any side effects or changes in participant condition.
- Documentation
- Accurately record participant information and enter study data (training provided).
- Protocol Adherence
- Follow study guidelines and learn how clinical trials are conducted ethically and safely.
- Team Collaboration
- Work with doctors, researchers, and lab teams in a supportive learning environment.
Qualifications
Minimum Qualifications
- Diploma or Bachelor’s degree in Nursing
- Registered with the Nursing Council and licensed to practice
- Recently completed internship (or within 1 year post-internship)
Required Experience
- No prior research experience required
- Clinical exposure during training/internship is sufficient
Compliance & Conduct
- Adhere to ICH-GCP, study protocols, and ACRN SOPs
- Maintain accurate, complete, and timely documentation
- Escalate any protocol deviations, safety concerns, or errors immediately
- Participate in required training and certification
Who should apply?
- Recently completed your nursing internship
- Registered nurse with a valid practicing license
- Curious about research and eager to learn
- No research experience? No problem, we’ll train you
Application Deadline: 6 May 2026
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