Key Responsibilities:

• • Assist in screening participants ≥ 14 years old with confirmed RR/MDR-TB.
• • Coordinate baseline and follow-up visits.
• • Oversee administration of oral trial regimens, compliance checks, and pill accountability.
• • Monitor adverse events and assist in required clinical procedures (e.g., vital signs, ECGs, spirometry).
• • Schedule and track participant visits to ensure retention.
• • Maintain accurate source documentation and ensure timely eCRF data entry.
• • Maintain essential documents in compliance with ICH-GCP.
• • Prepare monthly recruitment and screening reports.

Must have:

• • Bachelor's Degree in Nursing; Board Certified/Licensed Nurse.
• • Clinical experience of 1-2 years is strongly preferred.
• • Experience in TB,pulmonary,infectious disease or internal medicine preferred.
• • Clinical research experience strongly preferred
• • Stong clinical skills in TB and MDR-TB management.
• • Profecient in Microsoft Office applications
• • Strong organizational and communication skills