Overview: Monte Rosa Therapeutics is seeking a Director Quality GCP to provide strategic oversight of phase...-appropriate Quality GCP and GCLP activities, including GCP quality oversight of ongoing quality activities supporting active pre...
Associate Director, GCP Audit & Compliance provides strategic quality oversight to clinical, medical, and pharmacovigilance...’s degree in a scientific, health, or medical field (or equivalent). Minimum 15+ years of experience in GCP/GCLP/GVP Quality...
Job Description General/Position Summary The Director, Quality Oversight Lead within Global Clinical Quality (GCQ..., the Director will be responsible for providing quality oversight to Clinical Development and Biometrics functional areas...
Job Title: Associate Director, Clinical Program Quality Location: Cambridge, MA 02142 - Hybrid Duration: 12 Months... Compliance and Systems team to identify and mitigate GCP quality and compliance issues with potential impact across multiple...
Job Title: Associate Director, Clinical Program Quality Location: Cambridge, MA 02142 Duration: 12 Months Hybrid... Compliance and Systems team to identify and mitigate GCP quality and compliance issues with potential impact across multiple...
Associate Director, Clinical & Quality Process Compliance is responsible for ensuring the quality of processes and product... Quality/Compliance. Advanced knowledge of pharmaceutical development, medical affairs and GCP/GVP regulations including FDA...
Job Title: Associate Director, Clinical Program Quality Location: Cambridge, MA 02142 - Hybrid Duration: 12 Months... Compliance and Systems team to identify and mitigate GCP quality and compliance issues with potential impact across multiple...
Job Description: Job Title: Associate Director, Clinical Program Quality Location: Cambridge, MA Duration: 12... Compliance and Systems team to identify and mitigate GCP quality and compliance issues with potential impact across multiple...
Job Title: Associate Director, Clinical Program Quality Location: Cambridge, MA 02142 Duration: 12 Months Hybrid... Compliance and Systems team to identify and mitigate GCP quality and compliance issues with potential impact across multiple...
Cambridge, US; Gaithersburg, US; New Jersey, US | full time | Job ID: 9897 As Director, Clinical Quality Assurance... on implementing a proactive, risk-based quality strategy, ensuring GCP compliance, fostering a culture of quality within the Global...
Cambridge, US; Gaithersburg, US; New Jersey, US | full time | Job ID: 9893 Responsibilities The Associate Director... Clinical QA Compliance supports and oversees the proactive and risk-based Quality Strategy implementation in the clinical...
Associate Director, Clinical and Safety Quality Compliance is responsible for ensuring the quality of processes and product... Quality/Compliance. Advanced knowledge of pharmaceutical development, medical affairs and GCP/GVP regulations including FDA...
global Clinical Programs Quality organization, establishing a strategic leadership and oversight of the Takeda’s clinical... development programs and ensuring risk-based quality interventions and audits are performed for timely mitigations. Provide...
and other presentations . As the Sr. Manager GCP Clinical Quality reporting to the Senior Director GCP Quality, you will be partnering...'s risk based GCP compliance approach globally Support Quality Management System (QMS) including, but not be limited to: QA...
Job Description: Responsibilities Job Title: Director of Services Reports to: Head of Service and Delivery FLSA... Status: Exempt Job Summary The Director of Services is responsible for leading the customer onboarding team and ensuring...
with high standards of quality and consistency while maintaining compliance with GCP regulations. You will oversee Olema... and other presentations . About the Role Director, Clinical Monitoring Oversight As the Director, Clinical Monitoring Oversight...
a Senior Director of Medical Affairs to support our lead oncology program as it enters its first pivotal study. Reporting..., managing budgets and timelines, and ensuring high-quality deliverables across medical information, field operations...
The Senior Medical Director Clinical Development will lead the clinical team for a high-visibility program and report.... You will be responsible for: Lead cross-functional clinical program teams to deliver high-quality studies and research strategies, ensuring...
Job Description General Summary: The Medical Affairs Senior Director provides medical and scientific leadership... integrity Ensures compliance at country level with company policies, medical affairs SOPs, GCP and ICH Assesses local...
, Biometrics, the Associate Director of Clinical Data Management will be responsible for leading the clinical data management... at collaboration, and is passionate about ensuring high-quality clinical data to drive impactful decision-making. Your Role: Lead...