Manage all aspects of clinical trials from start-up through close-out, providing functional expertise to ensure that study timelines, costs and quality metrics are met and the study is conducted in compliance with the study protocol, SOPs, and applicable regulatory requirements. Responsible for selection of vendors/CROs and provide effective ongoing management to vendors/CROs.
Seeking a highly motivated Field Applications Scientist to join the Commercial Team. This role involves pre-sales enablement, bioinformatics data interpretation, and strategic territory engagement, supporting the Western United States. The ideal candidate will manage large territories and partner with commercial teams to drive business growth, providing technical support, conducting seminars, and offering experimental design consultations.
Support the expanding Clinical Trial portfolio at Oruka Therapeutics as the Manager of Clinical Data Management, providing data management support while maintaining high quality standards and compliance with regulations; lead data manager for 3 to 4 studies, reporting to the Sr. Director of Data Management.
We are seeking a Biostatistician to join our growing team. As a key member of our team, you’ll work closely with cross-functional groups to design and implement statistical methods and programming for clinical trials, while gaining valuable exposure to cutting-edge technologies in healthcare.
As the Clinical Program Director, you will design and execute strategies to generate high-quality evidence for regulatory approval, product validation, and therapy adoption. You'll shape pivotal clinical programs, influence product direction, and impact a company at the forefront of mental health innovation. You'll collaborate with cross-functional experts and KOLs to drive advancements in patient care.
The Translational Medical Scientist contributes to partnerships with clinicians, product managers, and key opinion leaders (KOLs) in applying genomic data to advance healthcare. This position focuses on the detection and analysis of circulating tumor DNA to inform clinical decisions and improve outcomes in patients with solid and hematological malignancies.
We are seeking a highly experienced Biology professional consultant to serve as a consultant on AI training data projects for leading AI model builders and enterprises. Your focus will be to define success criteria, review outputs, and provide targeted guidance to improve quality and speed — directly contributing to the successful delivery of domain-specific annotated datasets that meet the highest technical standards.
In this role, you will be a team member on one of the Therapeutic Area (TA) Quality teams and provide proactive, end to end quality oversight through various methods of risk-based quality management activities, including quality by design and real-time analysis of quality data/metrics. You will develop deep knowledge of the TA’s clinical trials and provide oversight and quality management of critical data and processes for global and local study teams and all clinical trial sites.
The Global Scientific Director for the Bioanalysis Laboratories will support the Bioanalytical Leadership team in developing a global scientific strategy and acquiring new clients. This individual will work with Business Development / Marketing, Operations and Project Management to identify, design and implement innovative and profitable solutions for our customers in our bioanalytical laboratories.
As the Associate Director or Director, Biostatistics you will lead critical statistical activities across one of our phase III clinical programs. You will provide strategic and technical leadership in the design, analysis, and interpretation of clinical trials in a dynamic, fast-paced organization. You will collaborate cross-functionally with various teams.