Explore 17 Remote Good Clinical Practices (gcp) Jobs
Join AbbVie as a Bilingual Clinical Research Associate II, where you will monitor clinical studies and ensure compliance with regulatory standards.
Join AbbVie as a Bilingual Clinical Research Associate II, responsible for overseeing clinical studies and ensuring compliance with regulatory standards.
Join AbbVie as a Bilingual Clinical Research Associate II to monitor and ensure compliance at clinical study sites.
Join AbbVie as a Clinical Research Associate I to support and manage clinical trials ensuring compliance with regulatory standards.
U.O.C
University of Chicago
Join the University of Chicago as a Research Assistant to support clinical studies focused on cancer prevention and health outcomes.
The Clinical Data Strategy and Operations Program Lead II at AbbVie is responsible for leading data science initiatives and ensuring successful delivery of clinical trial programs.
Join Tempus as an Associate Project Manager to enhance operational efficiency in cancer clinical trials.
The Quality and Regulatory Specialist ensures compliance with quality standards and federal regulations in a hybrid work environment.
The Clinical Research Associate I role involves managing clinical trials and ensuring compliance while working remotely.
Join MERIT CRO as a full-time Oncology Imaging Quality Control Specialist I, focusing on clinical data quality evaluation and support.
Join MERIT as an Oncology Project Manager to oversee clinical trial operations and ensure quality management throughout the study lifecycle.
D.M
Disc Medicine
Join Disc Medicine as an Associate Director/Director of Research Quality Assurance to lead compliance and quality oversight in a hybrid work environment.
Join Apogee Therapeutics as a Clinical Trial Manager to oversee global clinical trial programs and ensure compliance with regulatory standards.
Tempus is looking for a Medical Director to oversee high-priority studies in precision medicine.
The Senior Clinical Trial Manager oversees the execution and management of clinical studies, ensuring compliance and quality.