RemoteOtterRemoteOtterExplore 236 Remote Regulatory Submissions Jobs
S.H.U.L
Syneos Health UK Limited
The Regulatory Consultant - CMC will oversee global regulatory CMC for marketed small molecule products and collaborate with cross-functional teams.
ClinChoice
Join ClinChoice as a Senior Biostatistician to lead statistical strategy for clinical trials in a remote setting.
ClinChoice
Join ClinChoice as a Senior Manager Biostatistician Consultant, working directly with clients on clinical trial protocols and statistical analyses.
W.C.T
Worldwide Clinical Trials
Join Worldwide Clinical Trials as a Senior Clinical Research Associate focusing on oncology, where you will manage research activities and ensure compliance in a remote role.
NeoGenomics Laboratories
Join NeoGenomics as a Principal Scientist Algorithm Lead to lead the development of clinical NGS diagnostic algorithms in a remote position.
NeoGenomics Laboratories
Join NeoGenomics as an Associate Director of Bioinformatics Product to lead innovative solutions in precision oncology.
Intuitive
Join Intuitive as a Senior Clinical Scientist to develop clinical evaluation plans and reports for regulatory submissions in the medical device industry.
P.P.M
Praxis Precision Medicines
Lead the development and validation of analytical pipelines and statistical models as an Associate Director, Statistical Data Scientist.
B.F.S
BeiGene France Sarl
The Associate Manager, Regulatory Affairs will oversee regulatory projects and submissions to ensure compliance and timely approvals in the pharmaceutical industry.
Altimmune
Altimmune
The Vice President of Biometrics will lead statistical strategy and data management for Altimmune's clinical development portfolio, ensuring scientific integrity and regulatory compliance.
Jobgether
Seeking a Remote Project Team Leader to oversee clinical trial projects in a Biotech Division.
AbbVie
The Medical Writing Coordinator/Publisher II is responsible for coordinating and publishing clinical and regulatory documents at AbbVie.
S.B.G
Syner-G BioPharma Group
The Consultant I, Medical Writing is responsible for authoring regulatory documents and managing projects to support client regulatory strategies.
ClinChoice
Join ClinChoice as a Principal Statistical Programmer / Analyst Consultant to lead programming activities for oncology clinical trials.
B.F.S
BeiGene France Sarl
BeOne is looking for an Associate Director to lead clinical biomarker initiatives in oncology, driving strategic and operational leadership.