Independently performs, coordinates and oversees all aspects of the clinical site monitoring services, assessing protocol and regulatory compliance as per Alimentiv’s and sponsor’s standard processes, ICH/GCP guidelines and local regulation. Serves as the primary liaison between the
Alimentiv is seeking a Clinical Operations Lead to oversee a defined regional/global set of CRAs and investigator sites in line with GCP, protocol and regulatory requirements. The role coordinates CRA training, site visits, enrollment strategies and monitoring
Responsible for the clinical operations of a project within a defined regional/global level. Provides oversight of project deliverables, assigned Clinical Research Associate (CRAs) and Investigator sites in accordance with the Monitoring Plan, Protocol, Good Clinical Practice
Independently performs, coordinates and oversees all aspects of the clinical site monitoring services, assessing protocol and regulatory compliance as per Alimentiv’s and sponsor’s standard processes, ICH/GCP guidelines and local regulation. Serves as the primary liaison between the
We are proactively inviting qualified candidates to join our talent pool for anticipated Clinical Research Associate (CRA) needs. At Alimentiv, our CRA teams play a critical role in site monitoring and study management across our global clinical