Aga Khan University Hospitals in Karachi, Pakistan and Nairobi, Kenya are private, not-for-profit institutions providing high quality health care. The Main Hospitals serve as the principal sites for clinical training for the University's Medical Colleges and Schools of Nursing and Midwifery in Pakistan and East Africa. Our Vision of Aga Khan University Hospital, Nairobi is to be the premier, tertiary, teaching and referral health care facility in sub-Saharan Africa. ​For over fifty years, Aga Khan University Hospital, Nairobi (AKUH) has been taking care of families in East Africa. As a private, not-for-profit hospital, we strive to provide access to quality healthcare to all who need it. At AKUH, patients are our first priority. Our team of medical professionals, faculty and staff are here to provide you and your loved ones with the highest standards of healthcare. We are committed to working together to ensure that you and your family receive outstanding medical services, first-rate facilities and compassionate care. The Aga Khan University Hospital, Nairobi has set the standard for comprehensive healthcare and modern medical education in East Africa. Our dedicated staff, advanced facilities and state-of-the-art technologies have earned the hospital great reputation as a leading medical institution and teaching hospital in the region, and beyond. Patients benefit from our unique team-based approach to car​e, which enables you to benefit from the diverse expertise of our entire team of medical professionals. As the teaching hospital for Aga Khan University’s Medical College and School of Nursing and Midwifery, we practice an evidence-based approach to medicine, driven by the cutting-edge research conducted by our experienced faculty members. Our approach to care is guided by our core principles of Quality, Access, Impact and Relevance.​Job Summary The Clinical Research Nurse plays a crucial role in the conduct of clinical trials and research studies. Responsibilities encompass a wide range of activities aimed at ensuring the safety, well-being and compliance of research participants, as well as the integrity of the research data. Responsibilities Identify and recruit eligible participants for Phase ≥1 clinical trials. Screen potential participants based on specific inclusion and exclusion criteria. Explain the details of the Phase ≥1 clinical trial to potential participants. Obtain informed consent from participants, ensuring they understand the risks, benefits, and procedures involved, in compliance with Good Clinical Practice (GCP) and human subjects protection. Administer investigational drugs or treatment/other interventions to participants according to the study protocol. Monitor participants closely for any adverse reactions or side effects during and after drug administration. Conduct regular assessments of vital signs, such as blood pressure, heart rate, respiratory rate, and temperature. Document and report any abnormalities or changes in vital signs. Perform physical assessments and clinical evaluations as specified in the study protocol. Monitor and document any changes in participants' health status. Promptly report any adverse events or serious adverse events to the study investigator and appropriate regulatory authorities. Collaborate with the principal investigator, study coordinator, and other team members to ensure the smooth conduct of the trial. Provide regular updates on participant status and study progress. Ensure strict adherence to the study protocol and regulatory requirements. Document all study-related activities accurately and in accordance with Good Clinical Practice (GCP) guidelines. Collect and process blood samples for pharmacokinetic or other analysis, as specified in the study protocol. Educate participants about the purpose of the Phase ≥1 clinical trial, the investigational product, and potential side effects. Be trained and prepared to respond to medical emergencies that may arise during the trial. Maintain detailed and accurate records of all participant interactions, assessments, and procedures. Ensure compliance with regulatory requirements and assist in preparing for regulatory inspections. Follow safety guidelines and procedures to protect both participants and staff involved in the study. Any other assignment that is deemed appropriate for this level. Requirements Bachelors degree in Nursing OR Diploma in Nursing with at least 5 years’ research experience Current licensure with the Nursing Council of Kenya Certification in Basic Life Support (BLS) CITI/ Research training preferred Relevant Experience Minimum of 3 years’ experience as a nurse in a hospital setting in inpatient and/or outpatient services with demonstrated knowledge and competencies in nursing clinical practices applied to direct patient care Sound working knowledge of Good Clinical Practices (GCPSs), clinical trial processes, nursing patient care, biomaterials handling, and health safety practices Prior experience in operating basic medical equipment (e.g., infusion pump, ECG Machine, etc.) Personal Characteristics & Behaviours Excellent written and Verbal communication skills Ability to work within a multidisciplinary team Strong critical thinking and Analytical skills Ability to multitask and handle diverse sets of tasks for multiple studies and clinics simultaneously Demonstrate proactivity and ability to work with minimum supervision. Ability to be flexible and work in a variety of related roles Proficient in MS Office Empathetic, culturally sensitive with a high level of respect for colleagues, patients and their families