Director - Quality GCP - Boston

Monte Rosa Therapeutics is seeking a Director Quality GCP to provide strategic oversight of phase-appropriate Quality GCP and GCLP activities. · ...

Monte Rosa Therapeutics is seeking a Director Quality GCP to provide strategic oversight of phase-appropriate Quality GCP and GCLP activities. · ...

Monte Rosa Therapeutics is seeking a Director Quality GCP. The role requires strategic oversight of quality activities and close collaboration with industry leaders in Boston and Basel. · ...

Monte Rosa Therapeutics is seeking a · Director Quality GCP to provide strategic oversight of phase-appropriate quality activities. · Primary GCP Quality contact for identified vendors and investigator sites. · Autor key GCP qualidade SOPs and key reviewer for other quality proc ...

The GCP Quality Assurance candidate will manage activities related to the development, maintenance and oversight of GCP activities related to the Clinical Trial activities sponsored by the company. · The primary responsibilities will be to ensure both quality and compliance of c ...

The Senior Director, GCP Quality Oversight candidate will manage activities related to the development, maintenance and oversight of GCP activities related to the Clinical Trial activities sponsored by the company. · Bachelor's degree in life sciences, pharmacy, nursing, or a rel ...

The GCP Quality Assurance candidate will manage activities related to the development, maintenance and oversight of GCP activities related to the Clinical Trial activities sponsored by the company. · ...

We are a global quality leader who put people first and forge lasting relationships to bring deep impact in the industry. · We strive for excellence, aiming to be the number one choice for our clients and our employees. We are passionate about Continuous Improvement and are alway ...

We are seeking an Associate Director/Director, · Quality Assurance,GCP to join our team.We are building the GCP Quality function · to support Xenon's clinical development programs, · as well as expand quality initiatives across the company. · Ensure the Company's quality systems ...

+ Lead strategic quality oversight activities for clinical laboratory medical and PV suppliers · + Develop execute and continuously improve the global risk-based supplier audit program · + Conduct supplier audits end-to-end including planning execution reporting and CAPA follow ...

The Associate Director provides strategic quality oversight to clinical suppliers across Takeda's global network.Lead the risk-based supplier audit program and drive compliance insights. · BENEFITSWe understand compensation is an important factor as you consider the next step in ...

The Associate Director, GCP/GVP Supplier Quality provides strategic quality oversight to clinical, medical, and pharmacovigilance suppliers across Takeda's global network.You will lead the risk-based supplier audit program, drive compliance insights, and partner closely with stak ...

Kymera is a clinical-stage biotechnology company pioneering the field of targeted protein degradation (TPD) to develop medicines that address critical health problems and have the potential to dramatically improve patients' lives. · Lead the development and execution of the Clini ...

The purpose of this position is to ensure that clinical trial activities for all assigned projects are conducted in compliance with applicable regulations Good Clinical Practice GCP guidelines International Conference on Harmonization ICH and Policies Procedures In addition this ...

We are seeking an Associate Director/Director, Quality Assurance, GCP to join our team. We are building the GCP Quality function to support Xenon's clinical development programs, as well as expand quality initiatives across the company. · Ensure the Company's quality systems and ...

We are looking for a highly motivated Associate Director, GCP Clinical Quality Assurance support advancement of our clinical trials in metastatic melanoma and non-small cell lung cancer. · We are pioneering engineered cell and gene therapies to deliver transformative outcomes for ...

Responsible for execution and performance of Lantheus CQA quality system elements including GCP audit programs, · regulatory inspection preparation support, continuous improvement, and quality system procedural documents. · ...

We're expanding our portfolio and pipeline across oncology, neurology and cardiology.Lantheus CQA quality system elements including GCP audit programs, · regulatory inspection preparation support, · continuous improvement, · and quality system procedural documents. · ...

We are partnering with a well-established global biopharmaceutical organization seeking Clinical Quality Assurance Managers for Phase I–III programs. · Lead GCP audits investigator sites CROs vendors internal processes · Provide quality oversight Phase I–III clinical trials · ...

We are partnering with a well-established global biopharmaceutical organization seeking Clinical Quality Assurance Manager to play critical role in clinical compliance audit execution inspection readiness across Phase I–III programs. · ResponsibilitiesLead and execute GCP audits ...