Clinical Officer (2 Positions)

Job Detail

Screen and evaluate participants for inclusion/exclusion criteria according to the study protocol
Diagnose, treat, and monitor participants’ clinical conditions throughout the study
Explain study procedures, risks, and benefits to participants and support the consent process
Ensure all clinical procedures, interventions, and assessments comply with the study protocol
Identify, manage, and report adverse events (AEs/SAEs) promptly to the PI and regulatory authorities
Record clinical findings, laboratory results, and treatment details accurately in source documents and case report forms (CRFs)
Responsible for recruitment of patients, their assessment and management during follow up, responsible for patient care and wellbeing;
Implement and oversee quality assurance measures for clinical procedures and data accuracy
Supervise day-to-day clinic operations, including staff coordination, patient flow, and resource utilization
Ensuring proper daily laboratory operations including specimens correctly labelled, sent for processing, follow up on laboratory results and transfer to study forms;
Ensure all patients are followed up till discharge from the study and any patient who misses a clinic visit is followed up at home;
Supervising Study staff including Nurses, Laboratory Technicians and Home Visitors

Diploma Certificate/Transcript – Mandatory
Certification in Good Clinical Practice (GCP) and Human Subjects Protection (HSP) – Mandatory
Annual Practicing License – Mandatory
Ordinary and Advanced Level Certificates – Mandatory

• Good team work and communication skills • Competence in clinical assessments, diagnostic procedures, patient management, and protocol-driven interventions • Strong communication, documentation, problem-solving, teamwork, and attention to detail. • Proficiency in the local language(s) spoken in the study area is required – Mandatory

Important Procedure

No payments should be made during the application process.
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Application ends in 7d 16h 10min