Sr Clinical Research Prgm Coord 2
Core
Lead implementation of clinical trials for tuberculosis, HIV, and non-tuberculous mycobacteria (NTM) treatments, managing workflow, protocol execution, and regulatory compliance for local, national, and international studies.
Role type
Senior Clinical Research Program Coordinator
Builds
Clinical trial protocols, case report forms, regulatory filings, and study dissemination products
Domain
Infectious disease research (TB, HIV, NTM) / Clinical Trials
Required skills
Clinical trial coordination, protocol implementation, regulatory compliance (IRB), grant preparation, data quality management, international site coordination, adverse event reporting, manuscript writing
Preferred skills
Nursing degree, program coordination experience, STATA, large-scale research program management
Technologies
Microsoft Office Suite, research databases, STATA
Responsibilities
Lead team in completing research protocols; coordinate site activation and activities for international studies; prepare regulatory submissions (IRB, clinicaltrials.gov); conduct routine data quality checks; assist with grant preparation and budget justifications; supervise administrative and research staff
Seniority
Senior, hands-on IC with supervisory responsibilities