Explore 37 Remote Good Clinical Practices (gcp) Jobs
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.
The Senior Director, Global Clinical Development will lead clinical development initiatives and ensure compliance with regulatory standards.
The Manager of Clinical Systems is responsible for overseeing clinical system processes and ensuring compliance within a fast-paced biotechnology environment.
U.O.C
University of Chicago
The Senior Clinical Research Coordinator oversees and coordinates complex clinical trials, ensuring compliance and high standards in clinical research practices.
The Executive Medical Director will lead clinical research efforts in cardiovascular risk reduction related to obesity, managing trials and overseeing evidence generation.
E.L
Edwards Lifesciences
Join Edwards Lifesciences as a Senior Clinical Research Monitor to ensure the ethical conduct and regulatory compliance of clinical trials while enhancing patient outcomes.
The Project Manager will oversee the planning and execution of clinical trials, ensuring compliance and effective client communication.
The Clinical Data Strategy & Operations Program Lead II is responsible for leading clinical data management efforts and ensuring compliance with regulations while optimizing study execution.
Join Amgen as an R&D Supplier Governance Monitor to ensure quality and integrity in clinical trials worldwide.
The Clinical Research Associate II will manage clinical trial sites, ensuring compliance and data integrity while supporting patient recruitment.