... a Clinical Study Manager to join its Research and ... MissionsbrAs our Clinical Study Manager, you will be in charge of :br * STUDY MANAGEMENT : Design, set-up, coordinate, monitor and promote non-clinical clinical studiesbr * PROJECT MANAGEMENT : Responsible ...
... protocols for clinical studies. Contribute to the development of ... preparation of clinical development plans Drafting and review of clinical scientific documents such as IND, IND amendments, Investigator Brochures, Clinical Study Reports, Annual Reports and ...
... Manager is assigned to trial sites to ensure inspection readiness through compliance with the clinical trial protocol, company Standard Operating Procedures (SOP), Good Clinical Practice (GCP), and applicable regulations and guidelines from study start ...
... protocols for clinical studies. Contribute to the development of ... preparation of clinical development plans Drafting and review of clinical scientific documents such as IND, IND amendments, Investigator Brochures, Clinical Study Reports, Annual Reports and ...
... Real-World Late Phase Research Clinical Operations Lead, Line Manager or Project Manager, conduct clinical remote monitoring visits and other clinical research activities in accordance with Study Protocol, Standard Operating Procedures (SOPs), ...
... Real-World Late Phase Research Clinical Operations Lead, Line Manager or Project Manager, conduct clinical remote monitoring visits and other clinical research activities in accordance with Study Protocol, Standard Operating Procedures (SOPs), ...
... in collaboration with the Regional Clinical Nutrition Manager and the Director of Clinical and Wellness Support * Complies with ...
... ., Central Labs, ECG, adjudications..) within studies * Support implementation of data provisioning for usage in studies for clinical trial reporting with appropriate data ...
... bioanalytical data in support of clinical pre-clinical studies. Provides administrative support to project ... -up, organization, and maintenance of clinical study documentation (e.g., Study Files, CRFs, etc.) and guidelines ( ...
... site manager throughout all phases of a clinical research study, taking overall responsibility of allocated sites. Develops strong site relationships and ensures continuity of site relationships through all phases of the trial. Performs clinical study site ...