RemoteOtterRemoteOtterExplore 161 Remote Regulatory Submissions Jobs
Precision Medicine Group
Join Precision for Medicine as a Clinical Research Associate II or Senior CRA, focusing on Oncology studies in a remote position based in Italy.
AbbVie
The Senior Manager, Statistics will lead statistical efforts in the development of Rheumatology clinical trials.
Trust Wallet
Join Trust Wallet as a Paralegal on a 6-month contract to support the legal team with research and documentation.
Precisionmedicinegroup
Join Precision for Medicine as a Junior Start Up Lead, managing site start-up activities remotely across Europe.
NLC
NLC
Join a biotech startup as a Junior Project Manager focused on innovative cancer treatments, working remotely from the Netherlands.
Deciphera Pharmaceuticals
Join a dynamic Medical Writing team as a Principal Medical Writer, leading the development of clinical and regulatory documents.
Precision Medicine Group
Join Precision for Medicine as a Clinical Research Associate II, working remotely in the UK and contributing to innovative cancer therapies.
Precisionmedicinegroup
Join Precision for Medicine as a Clinical Research Associate II, a remote position based in Italy, focusing on monitoring and managing clinical studies in oncology.
NLC
NLC
Join a biotech startup as a Junior Project Manager, supporting innovative cancer treatment development in a part-time remote role.
Sirtex
The Senior Director, Global Clinical Development will lead clinical development initiatives and ensure compliance with regulatory standards.
B.B
bluebird bio
Join bluebird bio as a Sr./Principal Statistical Programmer, leading data analysis for clinical trials with minimal supervision.
Aurion Biotech
Aurion Biotech is looking for an Associate Director, Clinical Affairs to oversee clinical development initiatives and ensure compliance with regulatory standards.
WNR
WNR
Join Mass General Brigham as a Per Diem Clinical Research Assistant to support clinical studies through data collection and patient recruitment.
R.E
RGH Enterprises
The Senior Regulatory Affairs Specialist oversees regulatory compliance and product development consulting for medical devices and pharmaceuticals.
P.I
Parexel International
The Regulatory Affairs Consultant is responsible for developing CMC strategies and managing regulatory submissions to ensure compliance with health authority guidelines.