RemoteOtterRemoteOtterExplore 234 Remote Fda Regulations Jobs
JSC SCRI Holdings
The Research Training Manager oversees training operations for clinical trial research staff at SCRI, ensuring effective education and compliance with industry standards.
K.O
Kura Oncology
Join Kura Oncology as a Senior Director, Medical & Regulatory Writing to lead and oversee the medical writing team in the development of precision medicines for cancer treatment.
Westone Laboratories
Seeking a Quality & Regulatory Compliance Specialist to support the company's QMS and ensure compliance with ISO and FDA standards.
Inogen
Inogen
The Regulatory Affairs Specialist IV ensures compliance with global medical device regulations and manages regulatory submissions.
K.P
Kite Pharma
The Senior Manager, Kite Safety and Pharmacovigilance leads pharmacovigilance activities and safety analyses for Kite's cancer therapies.
Jobgether
We are looking for a remote Product Manager to lead the development of innovative SaaS solutions in microscopy testing.
Cleerly
Join Cleerly as a Principal Design Quality Engineer to ensure compliance and quality in software medical device development.
R.C
Real Chemistry
Real Chemistry is seeking a detail-oriented Editor to ensure editorial quality control of healthcare communications and marketing deliverables.
Indeed
Indeed
Join UniTriTeam as a Remote Clinical Research Coordinator to facilitate clinical trials and support remote patient interactions.
Celcuity
Celcuity
The Senior Auditor will lead and execute complex GxP audits, ensuring compliance and product quality in a remote setting.
Factored
Join Factor as a Pharma Legal Associate to draft and negotiate pharmaceutical agreements while collaborating with cross-functional teams.
A.T.P
Axiom Talent Platform
Seeking an experienced FDA Regulatory Attorney with expertise in Class III IVD and companion diagnostics.
Jobgether
The Clinical Program Manager will oversee global clinical studies, ensuring regulatory compliance and enhancing trial performance.
PSI CRO
The Associate Medical Writer will be responsible for creating and reviewing clinical documentation in a remote setting.
Madrigal
Madrigal
Join Madrigal as a GMP Quality Assurance Specialist to ensure compliance with quality standards in a biopharmaceutical setting.