Explore 87 Remote Good Clinical Practice (gcp) Jobs
Join our Life Sciences practice as a Solution Design Analyst, focusing on delivering eCOA solutions for clinical trials.
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Arcus Biosciences
The Senior TMF Specialist is responsible for managing regulatory documents for clinical trials in a remote contract position.
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Arcus Biosciences
The Senior TMF Specialist is responsible for managing regulatory documents for clinical trials, ensuring compliance with GCP and related guidelines.
RayzeBio
RayzeBio
The Director of Clinical Site Operations leads clinical trial execution and site management to ensure data quality and patient safety.
The Senior Manager, Project Management will lead project management initiatives to enhance operational efficiency and oversee a team of project managers in a fully remote setting.
Join Paradigm as a Clinical Trial Project Manager and oversee the execution of clinical trials while ensuring compliance and operational excellence.
C.H.M.G.O.F.P
Carbon Health Medical Group of Florida PA
Join Carbon Health as a Clinical Research Coordinator and support innovative clinical studies while ensuring adherence to regulatory standards.
The Associate Director, Clinical Trial Services manages a team overseeing oncology studies and ensures the successful delivery of clinical trials.
The Clinical Trial Associate II is responsible for coordinating clinical operations activities in a remote setting.
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MSD OU
The Country Lead Associate Director Clinical Research manages clinical trial execution and compliance in Saudi Arabia, ensuring effective collaboration with local teams and stakeholders.
The Site Support Solutions Manager EMEA leads a team to enhance clinical trial operations and ensure exceptional customer experiences.
The Specialist, Regulatory Operations will manage regulatory activities for clinical trials, ensuring compliance with U.S. regulations.
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Avalyn Pharma
The Senior Clinical Data Manager oversees data management activities across global clinical trials, ensuring data integrity and compliance.
Join Allucent as a Clinical Research Associate II to manage and monitor clinical trials, ensuring compliance and supporting junior team members.
Join Sarah Cannon Research Institute as a Regulatory Affairs Manager to oversee regulatory operations and ensure compliance for clinical trials.