Explore 36 Remote Fda Guidelines Jobs
C.B
Cogent Biosciences
Seeking an experienced medical writer to lead the development of clinical and regulatory documents in a biotechnology company.
Enveda is seeking a Director of Toxicology to lead drug development efforts and manage nonclinical toxicology programs.
G.S
Gilead Sciences
Join Gilead as a Senior Scientist to lead the impurities development team in biopharmaceutical analytical operations.
Rho is seeking a Clinical Research Associate II to manage site monitoring and ensure compliance with clinical trial protocols.
I.C
IMVT Corporation
Join Immunovant as an Associate Director of Biostatistics to lead statistical strategies in a remote, dynamic environment.
Kardigan
Kardigan
The Director of Scientific Communications will lead strategic communication efforts within a heart health company, focusing on scientific data and medical strategies.
The Clinical Study Manager oversees the planning, execution, and closing of clinical trials, ensuring compliance with regulations and protocols.
Lead the biostatistics efforts for projects and manage the Biostatistics and Statistical Programming department.
Lead biostatistics efforts and manage resources within the Biostatistics and Statistical Programming department.
.E.C.S
8 ECU CENER S.A
The Travel Clinical Research Coordinator I manages clinical studies, ensuring compliance and overseeing patient interactions while traveling extensively across the US.
The Remote Sr. Principal Statistician leads statistical analysis in the pharmaceutical industry, ensuring compliance with regulations and quality standards.
I.G
IntelliPro Group
Join as a Pharmaceutical Consultant Writer to provide medical writing direction and ensure compliance with regulatory standards.
M.I.L
Medline Industries, LP
Join Medline ReNewal as a Primary Inspection Technician, responsible for inspecting and assembling reprocessed medical devices.
M.S.D
Merck Sharp & Dohme
The Regional Medical Scientific Director engages in scientific exchange and supports the company's GI Immunology program while residing in the Great Lakes territory.
The Senior Analyst, Site Contracts is responsible for preparing and negotiating clinical trial agreements and ensuring timely amendments throughout the study lifecycle.