Explore 232 Remote Regulatory Submissions Jobs
Join NeoGenomics as an Associate Director of Bioinformatics Product to lead innovative solutions in precision oncology.
Join NeoGenomics as a Principal Scientist Algorithm Lead to lead the development of clinical NGS diagnostic algorithms in a remote position.
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.
Seeking a Remote Project Team Leader to oversee clinical trial projects in a Biotech Division.
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.
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.
M.M
Mind Medicine
Definium Therapeutics is seeking an Associate Director of Medical Writing to author clinical and regulatory documents and support clinical study execution.
The Director of Project Management at Sobi will lead strategic initiatives for the launch of pharmaceutical products, ensuring effective project management and cross-functional collaboration.
B.F.S
BeiGene France Sarl
The Associate Director, Scientific Programming will lead statistical programming efforts for oncology projects, ensuring regulatory compliance and high-quality deliverables.
SerenaGroup
SerenaGroup
SerenaGroups is looking for a Medical Writer to create clear and engaging content from complex medical information.