Global Head, Clinical Quality Assurance & Compliance
$265k - $300kJade Biosciences
A clinical-stage biotechnology company is seeking an Executive Director of Clinical Quality Assurance to oversee quality assurance for clinical trials. This remote role requires expertise in GCP, GPvP, and GLP, ensuring compliance with regulations. Responsibilities include providing QA oversight, leading risk-based audit strategies, and maintaining inspection readiness. The expected salary range is $265,000 - $300,000 based on experience and geography. #J-18808-Ljbffr Jade Biosciences
$240k - $300k
...peptide drugs. We are advancing a clinical‐stage pipeline of... ...innovators and financed by top-tier global life sciences investors. The... ...a Senior Director of GMP Quality Assurance (QA) to serve as a senior quality... .... This role verifies compliance with cGMP regulations, company...SuggestedContract work$240k - $300k
...peptide drugs. We are advancing a clinical‑stage pipeline of... ...seeking a Senior Director of GMP Quality Assurance (QA) to serve as a senior quality... ...leading, and executing the global GMP QA strategy in support... .... This role verifies compliance with cGMP regulations, company...SuggestedContract work$265k - $300k
Executive Director, Clinical Quality Assurance Boston; San Francisco; Seattle About Jade Biosciences... ...activities to ensure quality assurance and compliance of Jade sponsored clinical trials... ...agencies. Stay current on global regulations, industry trends, and best...SuggestedWork at officeRemote work- ...simple: to make really high quality essentials for really low prices... ...at Quince.THE ROLE Quality Assurance Director, ApparelThe Quality... ...regulatory standards across all global markets. The Director... ...textile performance, regulatory compliance), advanced inspection processes...SuggestedLocal area
- ...Position Title: Director of Quality Assurance Reports To: Head of Quality and Regulatory... ...Quality initiatives, ensuring compliance with US FDA regulations, ISO 13485, and global regulatory requirements. S/... ...Quality guidance for clinical studies to ensure GCP compliance...SuggestedFull timeContract workWork at officeLocal areaWorldwide
$245k - $280k
...Quality Assurance Director / Sr. Director (GVP/PV) Mavericks Wanted... ...Practices (GVP) quality and compliance program at Eidos Therapeutics... ...affairs, regulatory, commercial, clinical operations and outsourcing... ...organization. Current knowledge of global GVP regulations and...Contract workWork at officeFlexible hours- ...for Medicines360’s Quality and GXP activities... ...audits with the Head of Quality and Regulatory... ..., clinical studies, and regulatory... ...submissions Ensure GCP compliance, supplier qualification... ...years of Quality Assurance experience,... ...teams locally and globally across multiple time...Work at office
$140k - $190k
...inhibition of BAFF and APRIL may prove clinically meaningful. Vera Therapeutics was... ...Position Summary:The Senior Manager, Quality Assurance (QA), will report to the Director, QA... ...Support the oversight of the quality and compliance, primarily cell bank and biologics DS...Contract workFor contractorsWork experience placementFlexible hours$265k - $331k
...Revolution Medicines is a late-stage clinical oncology company developing novel... ...Executive Director (ED) of Global Patient Safety (GPS) Quality and Compliance to join our dynamic team. The ED... ...Action (CAPA) management, Quality Assurance (QA), and maintenance of Good Clinical...Full timeContract workLocal area$93.1k - $232.8k
...breakthrough treatments to patients faster.Drive global clinical trials from first site activation to... ..., and closeout—while balancing speed, quality, and cost. You will serve as the... ...lead cross-functional teams, and ensure compliance with ICH-GCP, regulatory requirements,...Full timeContract workPart timeWork at officeImmediate startWorldwide$180k - $350k
....00/yr We are seeking a Head of Quality & Regulatory Affairs to own... ...strategy as we advance from pre-clinical development into clinical... ...authority on quality, compliance, and risk. You will be a core... ...trade‑offs Interface with global regulators as needed (EMA, MHRA...$199.2k - $246.1k
...and continuous evolution of quality assurance strategies, policies, programs... ...quality standards and global health authority regulations... ...champion and model a culture of compliance and quality excellence across... ...and risk areas across clinical programs and drive development...Full timeContract workWork at officeLocal areaFlexible hoursShift work2 days per week3 days per week- ...President invites applications for an Associate Director of Audit Quality Assurance in Oakland, CA. This hybrid role leads the quality assurance... ..., and follow-up of internal audit quality reviews, ensuring compliance with professional standards, and supporting external quality...Work at office
$265k - $331k
Revolution Medicines in San Francisco seeks an Executive Director of GCP QA to oversee the global GCP quality strategy and ensure compliance across clinical development programs. The candidate will lead a QA team, oversee vendor quality management, and engage with regulatory...- ...Redwood City, CA seeks a Senior Director of Clinical Data Management to lead data management strategy and teams across global trials. You will set SOPs, manage budgets, and... ...data integrity in collaboration with clinical, quality, and regulatory partners. The role requires...
$220k - $235k
Caribou Biosciences is a leading clinical-stage CRISPR genome-editing... ...and activities supporting quality oversight towards GCP, GLP, and... ...improvement.Responsibilities:Compliance Oversight: Ensure that all... ...requirements.Provide Clinical Quality Assurance (GCP) strategic and technical...Local areaRemote workFlexible hours- Revolution Medicines is seeking a Senior leader to oversee Global Quality Systems Monitoring & Excellence, ensuring governance, compliance, and continuous improvement across the QMS at our Redwood City, CA headquarters. You will drive audit readiness, KPIs, and cross-functional...
$265k - $331k
Revolution Medicines is a late‑stage clinical oncology company developing novel targeted therapies... ...role that sets and executes the global GCP quality strategy across clinical development programs. The role ensures compliance with regulatory requirements, industry standards...Full timeContract work- ...Jade Biosciences is seeking a Director, GMP Quality Assurance to provide critical QA support across its product pipeline. This remote role requires oversight of GMP compliance and collaboration with CMC and cross-functional teams to ensure product quality standards....Remote work
- ...activities that lead to, and maintain compliance to/with Cutera’s Quality Management System and maintains... ...to ensure continued compliance with global regulatory and customer requirements.Lead and manage Cutera’s Quality Assurance department and employees to achieve...
$220k - $235k
A biopharmaceutical company in Berkeley is seeking a Quality Assurance Lead to develop and implement QA systems for clinical trials. The role requires overseeing compliance with GCP and GLP standards while managing audits and documentation reviews. Ideal candidates should...$112k - $140k
...development, and commercialization of clinically differentiated, high‑value healthcare... ...information for transplant patients. As the Quality Assurance (QA) Lead, you will partner across... ...to drive quality excellence, ensure compliance with applicable quality system regulations...Full time- CareDx, Inc. is seeking a Quality Assurance Lead to partner across multiple functions and drive quality excellence in a CLIA, FDA and GCLP... ...will implement and maintain quality system processes ensuring compliance across the lifecycle of our products. You will manage the...
$93k - $191k
Position Summary The National Tax Quality Assurance (NTQA) QRM Support Team Manager is... ...Participate in consultations with US and Global Tax Risk, Independence and Conflicts Network... ..., legal, or professional services risk/compliance; strong judgment and discretion...Contract workWork at officeLocal areaVisa sponsorship- A pharmaceutical company in San Francisco is seeking an Executive Director of Global Patient Safety Quality and Compliance to oversee pharmacovigilance practices. This key role involves developing quality management systems, ensuring regulatory compliance, and leading...
$160k - $180k
Olema Oncology is a clinical-stage biopharmaceutical... ...a $15 billion global market opportunity.Our... ...Associate Director, GMP Quality, reporting to the Head of GMP Quality, you... ...supporting Supplier compliance. In this role you... ...relate to GMP Quality Assurance Experience: Minimum...Work experience placementWork at officeFlexible hours$160k - $180k
...the Role Senior Manager, GCP Clinical Quality reporting to the Senior Director GCP Quality Assurance, you will be partnering with... ...study teams to ensure GCP/GVP compliance, assisting in identifying and... ...based GCP compliance approach globally Support Quality Management...Work at officeFlexible hours2 days per week$193k - $242k
...these patients. Alumis is hiring a Clinical Quality Assurance Director, (CONTRACTOR) reporting to... ...maintains the standards expected by global regulatory authorities. Essential... ...Ensure ongoing clinical programs are in compliance with applicable health authority regulations...For contractors$195k - $215k
...are currently seeking a Director of Clinical Quality Assurance to serve as the senior individual contributor... ...and protocols. Reporting to the Head of Quality, the Clinical QA Director... ...GCP-critical documents to verify compliance with GCP requirements Review and negotiate...Work at office3 days per week$195k - $215k
...Ray Therapeutics, Inc. is searching for a Director of Clinical Quality Assurance based in Berkeley, CA, to lead our clinical QA function. This pivotal role involves ensuring compliance with GCP regulations, managing clinical audits, and implementing quality oversight...Work at office
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