Chief Risk Officer Jobs in Bothell
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Search Results - Chief Risk Officer Jobs in Bothell
Systimmune-Bothell
The CDM will support and/or lead clinical database design, data collection and validation, data management, and reporting work for clinical trials. Additionally, the CDM will play a key role in overseeing CROs and vendors to meet study needs...
Bausch Health-Bothell
selection, qualification, and ongoing oversight planning• Oversee CRO and external vendor performance related to site management activities, including review of monitoring visit reports, tracking of key performance indicators, and escalation of performance...
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Systimmune-Bothell
including table/listing/figure shells, and review final SAR and CSR.
• Oversee and validate CRO programming activities, ensuring accuracy in internally or externally produced SDTM, ADaM, SAS tables, listings, and figures.
• Conducts quality control...
Immunome-Bothell
or 8 years (with a Masters) of biostatistics experience supporting clinical trials in the pharmaceutical, biotech, or CRO industry, or equivalent.A minimum of 2 years of leadership or people-management experience is preferred. Knowledge and SkillsPrior...
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Systimmune-Bothell
development, and CDx regulatory expectations, and can work effectively across R&D, clinical, regulatory, QA, and external CROs and central laboratories.
Key Responsibilities
IHC Assay & CDx Development
• Lead development of IHC-based CDx assays, from...
Immunome-Bothell
management, vendor governance, compliance monitoring, risk management, quality agreements, CAPA management, and inspection readiness for GxP suppliers and service providers, including CDMOs, CROs, contract laboratories, consultants, and other outsourced...
mindmatch.ai -
Systimmune-Bothell
Partner with Clinical Operations, Medical, Regulatory, Drug Safety, Biometrics, and Program Management to ensure financial accuracy behind trial-level assumptions.
• Oversee financial aspects of contracts with CROs, laboratories, vendors, and other...
Immunome-Bothell
activities, including CROs and central labs. Demonstrated experience with trial documentation and Trial Master File management. Knowledge and SkillsWorking knowledge of clinical trial processes, and ICH-GCP. Strong organizational skills with the ability...
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YO AI Labs-Seattle, 12 mi from Bothell
claims.
• Prepare structured, guideline-based written feedback.
Required Qualifications
• 5+ years of Regulatory Affairs experience in the pharmaceutical, biotech, or CRO industry.
• Experience with clinical submissions, regulatory documentation...
careers-page.com -
IQVIA-Seattle, 12 mi from Bothell
experience (CRO/Pharmaceutical), and/or sales experience, including 10 years of management responsibility Req OrEquivalent combination of education, training and experience ReqProven track record at developing mid-level and high-level contactsStrategic...
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