Senior Director, GCP - Somerville

Generate:Biomedicines is a new kind of therapeutics company pioneering Generative Biology to create breakthrough medicines. We are seeking collaborative problem solvers to join us. · Lead GCP and GPV quality strategy and execution across clinical programs, ensuring compliance wit ...

We are seeking a Senior Director, GCP & GPV to lead clinical quality and pharmacovigilance strategy across development-stage programs. This role ensures global Good Clinical Practice (GCP) and Good Pharmacovigilance Practice (GPV) compliance. · BS or advanced degree in biology, c ...

We are seeking collaborative, relentless problem solvers to join us in pioneering Generative Biology to create breakthrough medicines where novel therapeutics are computationally generated. · ...

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 ...

Monte Rosa Therapeutics seeks a Director Quality GCP to provide strategic oversight of quality activities supporting active pre-clinical and clinical programs. · ...

The Associate Director, Research & Clinical Development Quality Assurance (R&CD QA) will provide program-level quality oversight and strategic support across Sarepta's Clinical Development and Real-World Evidence portfolio. · ...

Job summary: · Sarepta Therapeutics is looking for an Associate Director to provide program-level quality oversight and strategic support across their Clinical Development and Real-World Evidence portfolio. · ...

Are you looking for a patient-focused, innovation-driven company that will inspire you and empower you to shine? Join us as an Associate Director, GCP Compliance in our Cambridge, MA office. · ...

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 ...

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 Associate Director provides strategic quality oversight to clinical suppliers across Takeda's network. · Lead strategic quality oversight activities for clinical suppliers · Develop and execute the global risk-based supplier audit program · Conduct supplier audits end-to-end ...

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 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 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 ...

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 ...

+ 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, 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 ...