Explore 11 Remote Gcp Guidelines Jobs
Care Access is seeking a full-time remote Source Document Specialist to create and manage source documents for clinical trials.
The Associate Director, Global Site Management oversees the strategic direction and execution of clinical site management within a therapeutic area.
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WEP Clinical
Join WEP Clinical as a Quality Assurance Associate to ensure compliance with GMP and GDP standards while supporting the Quality team.
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DVA DaVita
Seeking a Regulatory Affairs Administrative Assistant to manage regulatory documents and support clinical trials at DaVita Clinical Research.
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Entrada Therapeutics
The Clinical Compliance Consultant will lead GCP compliance strategies and support clinical trial operations in a part-time role.
The Source Document Specialist will create and manage source documents for clinical trials in a fully remote role.
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St. Jude Children's Research Hospital
The Clinical Research Monitor ensures compliance and accuracy in clinical research studies while managing documentation and communication with study teams.
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Disc Medicine
Disc Medicine is seeking a Clinical Trial Manager to lead early-phase clinical research studies in a hybrid work environment.
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Carbon Health Technologies
Carbon Health is seeking a Clinical Research Principal Investigator to lead clinical trials and innovate patient care.
The Senior Director, Clinical Operations will oversee global clinical trials and lead cross-functional teams to ensure compliance and efficiency in clinical operations.
The Director of Clinical Operations will oversee global clinical trials and ensure compliance with regulations while leading cross-functional teams.
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