Associate GCP/GLP QA Director - Alameda, CA

This key role drives consistency across QA systems and processes for the Clinical QA team, identifying issues and risks, escalating in a timely fashion, and aligning metrics that provide input into a compliance scorecard for Clinical programs. · Responsible for designing and coor ...

This role drives consistency across QA systems and processes for the Clinical QA team, identifying issues and risks. · Designs and coordinates Quality systems across Clinical Quality Assurance. · ...

About Acadia Pharmaceuticals Acadia is committed to turning scientific promise into meaningful innovation that makes the difference for underserved neurological and rare disease communities around the world This position plays a critical role in protecting data integrity and regu ...

The Associate Director leads the planning execution reporting of internal external GLP GCP audits ensuring compliance with U.S international regulations driving continuous improvement in quality systems. · Plan schedule coordinate conduct internal external GLP GCP audits of compa ...

Mirum Pharmaceuticals is a biopharmaceutical company dedicated to transforming the treatment of rare diseases. · ...

Mirum Pharmaceuticals is hiring an Associate Director of GCP/GVP/GLP-QA to support clinical study programs and ensure quality standards in compliance with regulatory requirements. · Bachelor's Degree in a scientific discipline. · 10-12 years of experience in the pharmaceutical in ...

· MISSION · Mirum Pharmaceuticals is a biopharmaceutical company dedicated to transforming the treatment of rare diseases. We are passionate about advancing scientific discoveries to become important medicines for rare disease patients. We are collaborative, creative, and experi ...

Mirum Pharmaceuticals is a biopharmaceutical company dedicated to transforming the treatment of rare diseases. · ...

The Associate Director of GCP/GVP/GLP-QA is responsible for supporting Mirum's clinical study programs as the GCP-QA representative on the study management team; managing activities involving GCP quality assurance and compliance with applicable regulatory requirements; · QUALIFIC ...

Mirum Pharmaceuticals is a biopharmaceutical company dedicated to transforming the treatment of rare diseases. · The Associate Director of GCP/GVP/GLP-QA is responsible for supporting Mirum's clinical study programs as the GCP-QA representative on the study management team; · man ...

We are seeking an experienced Associate Director / Director of GCP Quality Assurance to provide strategic and operational quality oversight of clinical studies and vendor programs. · Provide quality oversight and GCP guidance to clinical study teams. · Evaluate clinical trial doc ...

An established biopharmaceutical organization in the South San Francisco area is seeking an experienced Senior Director of GCP Quality Assurance to provide strategic and operational oversight of clinical programs and external partners. · This on-site leadership role ensures compl ...

+We are seeking an experienced, dynamic, and results-driven Associate Director / Director of GCP Quality Assurance to provide strategic and operational quality oversight of clinical studies and vendor programs.+ · +Provide quality oversight and GCP guidance to clinical study team ...

+Job summary · An established biopharmaceutical organization in the South San Francisco area is seeking an experienced Senior Director of GCP Quality Assurance to provide strategic and operational oversight of clinical programs and external partners.ResponsibilitiesProvide GCP ov ...

We are seeking an experienced, dynamic, and results-driven Associate Director / Director of GCP Quality Assurance our on-site team in South San Francisco. This role is critical in providing both strategic and operational quality oversight of clinical studies and vendor programs, ...

We are seeking an experienced Senior Director who will provide quality oversight and GCP guidance to clinical study teams and CROs/vendors to ensure compliance with ICH GCP, applicable regulatory requirements, · Provide quality oversight and GCP guidance to clinical study teams a ...

Job Description · MastarRec is recruiting a Senior Research Scientist to support biotechnology and life sciences organizations across the United States to join our cutting-edge research team driving innovation in genomics, transcriptomics, and multi-omics data analysis. · In this ...

The Director of Engineering R&D Infrastructure Operations will lead Siemens Digital Industries Software's worldwide facilities planning and operations. · ...

The Data Scientist will be responsible for advancing the company's AI/ML strategy and delivering high-impact data-driven solutions. · ...

The Clinical Supplies Manager II oversees all aspects of clinical supply management including packaging, labeling, monitor inventory levels, · and distribution by interacting with internal and external supply partners/vendors to ensure supply of IMP are sufficient at depots · and ...