KEY ROLES AND RESPONSIBILITIES:
1. Obtain informed consent from study participants.
2. Conduct physical examinations and take patient histories.
3. Make trial-related medical decisions.
4. Report Serious Adverse Events (SAE) and Adverse Events (AE).
5. Collect patient locator details.
6. Schedule follow-up appointments.
7. Review and manage resource documentation.
8. Maintain investigational product receipt/return records.
9. Maintain the essential regulatory document file.
10. Perform data collection and resolve queries as needed.
PERSON SPECIFICATIONS:
Qualifications:
• Minimum of a Diploma in Clinical Medicine from a recognized University/Institution.
• Registered with the Allied Health Professionals Council (AHPC).
• Willingness to commit to at least 2 years of service (no gender discrimination).
Experience:
• At least 3 years of clinical medical practice experience.
Knowledge:
• Strong knowledge of clinical medicine principles, procedures, and techniques.
• Knowledge of medicines, hygiene management, and infection prevention and control
(IPC) protocols.
Skills:
• Proficient in applying clinical medicine principles and procedures in patient evaluation
and treatment.
• Skilled in prescribing appropriate medications.
• Excellent interpersonal and communication skills.
• Proficient in both written and spoken English.
Abilities:
• Ability to maintain patient confidentiality and adhere to professional codes of conduct.
• Ability to treat all patients and staff with respect, without prejudice.
• Ability to provide high-quality, ethical, and compassionate care that prioritizes the needs
of the patient.
• Ability to maintain accurate and detailed records.
• Ability to adapt to changing conditions and manage stress effectively.
• Proficient in local languages spoken in the area; Ateso, Lugwere, and Kumam.