Remote Pharmaceuticals Jobs • ICH-GCP

The Clinical Trial Manager is responsible for the planning, conduct and oversight of the operational portion of clinical studies and ensures studies are conducted in accordance with the protocol, SOPs, ICH-GCP and all applicable regulatory requirements. They will serve as the primary clinical point of contact with the client. They will also develop study related clinical documents, training needs for CRAs and third-party vendors, and recruitment/retention strategies.

The L-LTM role is responsible for ensuring top-quality end-to-end trial delivery at a country level, managing the consistency of Local Trial Management duties and processes. The L-LTM will serve as the country-level single point of contact on the study for internal partners, managing and overseeing Central IRB and local vendors, executing local milestones, and ensuring inspection readiness.