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Kyverna Therapeutics
Join Kyverna Therapeutics as a Director of Quality Compliance to lead GxP quality systems and risk management in a hybrid role.
S.S
1S2 Seagen
The Clinical Data Scientist manages CDIS deliverables for clinical trials, ensuring data quality and compliance.
AbbVie
The Senior Manager in Regulatory Affairs will oversee US advertising and promotion compliance for AbbVie’s immunology and dermatology products.
Natera
The Sr. Clinical Biospecimens Operations Associate oversees biosample activities for clinical research studies, ensuring compliance and effective project management.
PSI CRO
The Principal Statistician will lead statistical activities in global clinical trials, collaborating with various international teams.
D.T
Dyne Therapeutics
The Associate Director, Medical Writing is responsible for preparing high-quality clinical and regulatory documents for Dyne Therapeutics.
PROCEPT BioRobotics
Join PROCEPT BioRobotics as a Senior Clinical Research Associate, overseeing clinical trials and ensuring regulatory compliance.
Natera
The Clinical Trial Manager will oversee all aspects of oncology clinical trials, ensuring compliance and efficient management.
Sobi
The Senior Manager will oversee regulatory compliance for advertising and promotional materials in the pharmaceutical industry.
Artera
Join Artera as a Systems Engineer to lead engineering activities ensuring compliance and effectiveness in medical AI solutions.
Natera
The Sr. Clinical Biospecimen Operations Associate manages biosample activities for clinical studies, ensuring compliance and operational efficiency.
Oura
Oura is seeking an Associate General Counsel to lead regulatory compliance and privacy initiatives for their innovative health technology.
S.P
Strive Pharmacy
The Content Compliance Specialist ensures all content at Strive Pharmacy is compliant with regulations and aligned with business objectives.
ClinChoice
Join ClinChoice as a Senior/Principal Statistical Programmer Consultant, working remotely in Canada.
RQM+
The Staff Toxicologist will lead toxicological risk assessments and regulatory submissions for medical devices.