Explore 20 Remote Ema Jobs
The ePRO Manager will lead the design and oversight of electronic Patient Reported Outcomes systems in clinical trials.
The Clinical Trial Safety Reporting Administrator ensures the timely and compliant submission of safety reports for clinical trials.
The Vice President of Regulatory Affairs will lead global regulatory strategies and submissions for late-stage biopharma programs in a remote role.
Join ClinChoice as a Global Labeling Lead Consultant, providing strategic support in pharmaceutical labeling while working remotely.
P.I
Parexel International
Join Parexel as a Senior Clinical Research Associate I to manage oncology clinical sites in the Paris region.
B.M.G.F.U.O
Bill & Melinda Gates Foundation - UK Office
The Senior Officer, Regulatory Affairs will manage grants aimed at optimizing regulatory systems for medical products in low-income countries.
Join Amgen as a Global Regulatory Policy and Intelligence Senior Manager to lead and influence regulatory strategies that impact patient care.
I.C
IMVT Corporation
Immunovant is seeking a Senior Director for Clinical Quality Assurance to lead quality efforts and ensure compliance with global regulations.
Join Syner-G BioPharma Group as a Validation Engineer to ensure compliance and enhance quality systems in life sciences.
Join ClinChoice as a Clinical Data Management Lead Consultant, overseeing clinical data management processes and leading a team.
The Sr. Director, Quality Systems will lead the Quality Systems team and ensure compliance with GxP operations in a temporary role.
Join our team as a Project Manager/Senior Manager in Regulatory Affairs to lead regulatory activities for product development and compliance.
The Senior Manager, Medical Writing will oversee document development and manage medical writing activities for drug marketing applications.