RemoteOtterRemoteOtterExplore 46 Remote Good Clinical Practice (gcp) Jobs
N-Power Medicine
The Medical Director, Clinical Science will lead the design and development of clinical research programs in a remote setting.
AbbVie
The Medical/Scientific Director will lead pipeline-related medical affairs activities in rheumatology, providing strategic input and ensuring compliance with regulations.
GondolaBio
GondolaBio is seeking a Senior Director of Quality Assurance to lead GCP activities for clinical trials and ensure compliance with regulatory standards.
E.L
Edwards Lifesciences
The Clinical Research Specialist is responsible for managing clinical trials and ensuring compliance with regulatory standards to improve patient outcomes in cardiovascular therapies.
P.I
Parexel International
The Study Operations Manager I oversees clinical study management and ensures compliance with regulatory standards while leading local study teams.
W.C
WEP Clinical
Join our team as a Mobile Research Nurse, providing essential nursing care and supporting clinical research protocols.
ELLIGO HEALTH RESEARCH
The Project Manager oversees clinical trial projects, ensuring successful delivery and client satisfaction.
Vitalief
Join Vitalief as a Clinical Research Coordinator to support decentralized clinical trials in a fully remote role.
Paradigm Health
Seeking an experienced Clinical Trial Project Manager to oversee clinical trials and ensure compliance and timely delivery.
Natera
The Senior Clinical Trial Manager will oversee all aspects of clinical trials, ensuring compliance and effective project management.
I.T
iRhythm Technologies
Join iRhythm as a Clinical Research Project Manager to lead and execute clinical research initiatives.
Allucent
Join Allucent as a Senior Clinical Research Associate Contractor to oversee clinical trials and ensure compliance with regulations.
Precisionmedicinegroup
The TMF Lead II oversees and manages the eTMF for clinical studies, ensuring compliance with regulatory standards.
Precision for Medicine
The TMF Lead II oversees and manages the eTMF for clinical studies, ensuring compliance with regulatory standards.
MCRA
The Director, Clinical Affairs will oversee clinical trials and ensure compliance with regulatory requirements while supporting the CRO leadership team.