RemoteOtterRemoteOtterExplore 19 Remote Regulatory Documentation Jobs
U.T.U.O.B.C
UBC The University of British Columbia
The Research Coordinator will manage a multicenter clinical trial to improve outcomes for preterm infants, overseeing all trial activities and data management.
M.O
MSD OU
The Clinical Research Specialist ensures compliance and performance in clinical trials, managing site relationships and monitoring activities.
ProTrials Research
The Clinical Research Associate is responsible for monitoring clinical studies and ensuring the success of clinical trial operations.
Amgen
The Regulatory Affairs Senior Associate role focuses on managing regulatory strategies and documentation for US promotional materials within a leading biotechnology company.
Indero
The Senior Project Coordinator provides support for site activation activities in clinical trials and may mentor junior coordinators.
M.O
MSD OU
The Senior Clinical Site Executive oversees clinical study sites, ensuring compliance and performance while managing relationships and monitoring activities.
AbbVie
The Statistical Analyst role involves leading the analysis and reporting of clinical trial data in a remote setting.
Jacuzzi Group
Join Jacuzzi Group as an Environmental, Health and Safety (EHS) Specialist to ensure a safe and compliant work environment.
M.O
MSD OU
The Senior Clinical Research Associate manages clinical research sites, ensuring compliance and performance throughout the study phases.
Pine Gate Renewables
Join Pine Gate Renewables as an Associate Project Manager to support solar project development and enhance your career in the renewable energy sector.
Faro Health
Join Faro Health as a Medical Writing Specialist to shape the future of medical writing with AI-driven solutions.
WNR
WNR
Join the Mass General Brigham team as a Clinical Investigation Technician, supporting research studies in sleep and circadian disorders.
X.V.M.S
591x Varian Medical Systems
The CT Clinical Education Specialist will provide expert training on Siemens CT Imaging systems, requiring extensive travel and strong communication skills.
Pharma Universe
The Clinical Research Associate II - Senior CRA conducts site visits and ensures compliance with clinical research protocols in Czechia.
T.W.A.C
Trilogy Writing and Consulting
Join Trilogy Writing & Consulting as a Medical Writing Manager to oversee a team and ensure quality regulatory documentation.