Explore 46 Remote Good Clinical Practices (gcp) Jobs
W.C.T.L
Worldwide Clinical Trials Limited
The Site Activation Manager oversees site activation project management and ensures compliance with regulations within the CNS therapeutic area.
The Clinical Research Associate II will manage and support clinical trials in oncology while ensuring compliance and data integrity.
The Clinical Research Associate I will engage with clinical trial sites to ensure compliance and quality in study execution while working remotely.
The Clinical Research Associate I will work remotely to enhance clinical trial performance and data integrity.
The Project Manager I oversees project management operations and supports clinical trials in a fully remote capacity.
The Senior Clinical Research Associate will drive the execution of clinical studies in oncology, ensuring compliance with regulations and mentoring junior staff.
The Clinical Research Associate II is responsible for ensuring the successful conduct of clinical trials in oncology, focusing on data integrity and compliance.
The Senior Clinical Research Associate will ensure the successful execution of clinical research protocols and manage site monitoring activities.
The Clinical Research Associate II is responsible for overseeing clinical trials and ensuring compliance with regulatory standards while enhancing site engagement.
The Senior Clinical Research Associate will ensure successful execution of clinical studies at AbbVie, focusing on site management and compliance.
The International Medical Director for Cardiovascular in JAPAC will lead medical strategy and execution across the region.
The Clinical Project Manager oversees the planning and execution of clinical investigations while ensuring compliance and maintaining client relationships.
The Clinical Study Manager will oversee clinical study operations to ensure compliance and quality in research projects at Foresight Diagnostics.
E.L
Edwards Lifesciences
The Senior Clinical Research Monitor ensures ethical conduct and regulatory compliance of clinical trials while monitoring data accuracy and patient safety.
Join MERIT as a full-time Imaging Quality Control Specialist, focusing on clinical trial data quality evaluation and analysis.