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Associate Director Clinical Operations Biotech Jobs in Oregon

OR

$343K - $365K/yr

... Operations to support integrated and strategic trial execution. * Regulatory: Provide scientific ... Minimum of 4+ years clinical development experience within the pharmaceutical or biotech industry ...

$183K - $223K/yr

... Pharma/Biotech industry or medical communication agency or equivalent experience * In depth ... Strong understanding of clinical trial conduct, real-world data generation and other data sources ...

The Associate Director of R&D Portfolio Operations & Insights will drive the design ... Minimum of 10 years of program management experience in biotech space and educational background in ...

Position Summary: The Associate Director, Medical Writing is responsible for oversight and ... clinical, regulatory, and scientific documents within the biotechnology or pharmaceutical industry.

Collaborate with R&D, biostatistics, clinical operations, and HEOR on protocol development ... At least 3 years of clinical trial experience in academia, biopharma, biotech, diagnostics, or an ...

Clinical Services Director - RN PRN; Remote role with travel nationwide for accepted assignments ... Responsible for clinical quality and or administrative (operational) activities as assigned in ...

Clinical Services Director - RN PRN; Remote role with travel nationwide for accepted assignments ... Responsible for clinical quality and or administrative (operational) activities as assigned in ...

... clinical trials, real-world evidence, and companion diagnostics. Responsibilities: Strategic ... biotech, and technology companies. o Lead cross-functional deal teams from initial outreach through ...

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QA Associate Director: Clinical Ops & Compliance (Bend)

Serán BioScience

Bend, OR • On-site

Full-time

Posted 24 days ago


Job description

Serán BioScience is seeking an Associate Director of Quality Assurance to oversee day-to-day QA operations, clinical manufacturing oversight, and warehouse activities, including disposition of raw materials and drug products. The role requires a results-driven QA leader with broad regulatory and quality systems experience.

You will lead continuous improvement, manage investigations, CAPAs, and inspections, mentor staff, and collaborate across functions to maintain cGMP compliance and timely

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