The consultant will support the design and implementation of social and behavioral science activities integrated within diagnostic validation studies for Ebola virus disease. They will collaborate with stakeholders to ensure community perspectives and user needs are incorporated into study design, execution, and dissemination.
The consultant will provide operational and technical support for the planning, monitoring, and execution of in vitro diagnostic clinical validation studies in global settings. Responsibilities include ensuring compliance with GCP and GCLP standards, managing study documentation, and facilitating communication with research stakeholders.
The Regional Clinical Officer provides technical support, mentorship, and supervision to health facilities to improve malaria diagnosis and case management. They also coordinate with regional health bureaus to plan, implement, and monitor malaria services and quality assurance programs.
The Global Head of CMC provides leadership and technical oversight for all CMC and non-clinical toxicology activities within the CVIA portfolio to ensure vaccine quality and regulatory compliance. This role manages cross-functional teams, oversees resource allocation, and conducts technical due diligence for partnerships to support vaccine development and delivery.
Consultants will provide technical expertise in infectious disease surveillance, including strategic planning, landscape analysis, and the design of outbreak detection systems. They will also support governments in integrating AI into health decision-making and facilitate capacity-building workshops.
The Ward Coordinator will manage malaria elimination activities at the ward level, focusing on surveillance, case reporting, and field team supervision. They are responsible for coordinating with municipal health teams and implementing ward-specific operational plans to achieve health indicators.
