Director of Study Quality & Compliance, Toxicology
Novartis Pharma Schweiz
Novartis Pharma Schweiz is seeking a Director to lead the Study Quality and Compliance team within the PCS Toxicology line. This hybrid role focuses on establishing strategy, overseeing GLP-compliant data management, and driving the implementation of tracking and analytics software across toxicology studies. The position requires an advanced degree in biology or related field with extensive pharma/toxicology experience, plus proven leadership. #J-18808-Ljbffr Novartis Pharma Schweiz
$185.5k - $344.5k
Job Description Summary Location: Cambridge, MA | Internal: Director | LI#-Hybrid This role oversees the Study Quality and Compliance team within the Toxicology line function of Preclinical Safety (PCS). The team is responsible for handling samples and data associated...Suggested$137.8k - $206.8k
General Summary The Senior Manager, Clinical Study Quality Lead provides study-level quality oversight for assigned clinical trials to help ensure they are conducted in compliance with Good Clinical Practice (GCP), applicable global regulations, study protocols, and Vertex...SuggestedSummer workRemote workFlexible hours2 days per week$160.6k - $240.8k
## Clinical Study Quality Lead, Associate DirectorApplylocations: Boston, MAtime type: Full... ...Clinical Study Quality Lead (SQL), Associate Director is responsible for advanced quality... ...identifying and communicating compliance risks and overseeing action plans to mitigate...SuggestedWork experience placementSummer workWork at officeRemote workFlexible hours2 days per week$252k - $269k
...Clinical Quality Assurance Senior Leader provides strategic leadership and operational... ...GLP/GCP/GVP quality programs to ensure compliance across global clinical trials. This leader... ...representative on program teams, sub teams, and study teams. Clinical Quality System Ownership...SuggestedLocal areaWorldwide- Senior Director, GCP Quality Oversight at Bicara Therapeutics Position Overview The Senior Director... ...include ensuring quality and compliance of company-sponsored clinical trials with... ...applicable laws. Conduct thorough reviews of study-related documentation, including...SuggestedContract workWork at officeLocal area3 days per week
$156.6k - $234.8k
...Description General Summary The Associate Director, GMP Operational Quality is responsible for oversight of team... ...of quality assurance and compliance. The incumbent is responsible for development... ...risks and collaborates with study team in development of risk mitigation...Work experience placementSummer workRemote workFlexible hoursDay shift2 days per week$160k - $187k
Senior Manager, Clinical Quality Assurance Boston, MA or Remote Responsibilities... ...Reporting to the Executive Director of Quality Assurance, the... ...that provide quality and compliance oversight utilizing proactive... ...partnerships with clinical study teams to provide GCP...Summer holidayWork at officeRemote workHome office- Vertex Pharmaceuticals is seeking a Clinical Study Quality Lead, Associate Director in Boston to oversee advanced quality assurance in clinical trials. Responsibilities include managing compliance with GCP standards, risk management, and coordinating with multiple stakeholders...
$265k - $300k
...LinkedIn. Role Overview The Executive Director, Clinical Quality Assurance (CQA) will be responsible... ...activities to ensure quality assurance and compliance of Jade sponsored clinical trials... ...Consent Forms (ICFs), Clinical Study Reports (CSRs), and other clinical trial...Work at officeRemote work- We are seeking an experienced Clinical Quality Assurance (CQA) Manager to lead and execute... ..., conducting GCP audits, assessing compliance with global regulatory requirements, and... ...broad range of audits, including: Clinical Study Audits Vendor and CRO Audits Clinical System...
$200k - $245k
...Summary of Position: Position Responsibilities Support global Quality Management System (QMS) transition from clinical-stage... ...for commercial operations. Establish and drive a proactive compliance framework that ensures sustained inspection readiness and supports...$120 - $170 per hour
Associate Director, Clinical Program Quality Leader Base pay range: $120.00/hr - $170.00/hr Location: Cambridge... ...of significant quality and compliance risks to key stakeholders and Management... ...Assume complex assignments on issues or studies where there is no precedent. Mentor...Temporary workFor contractorsWork at officeImmediate startNight shift2 days per week$192.6k - $260.6k
Overview Director, Clinical Quality Risk & Portfolio Oversight leads enterprise-wide quality intelligence, portfolio risk... ...emerging quality signals, systemic compliance risks, and operational trends across studies, vendors, computerized systems, audits, inspections...Local areaRemote workShift work$170k - $180k
...our shared mission unites us across functions and geographies. POSITION: Quality Systems Manager The Quality Systems Manager will be responsible for overseeing and ensuring compliance with current Good Practices (GxP) for applicable GxP systems, including document...Work at officeRemote workWorldwideFlexible hours- Zai Lab seeks a Clinical QC Manager to lead quality control of multicenter trials and ensure adherence to study protocols, GCP, and company procedures. You will partner... ...resolution. The role reports to the Executive Director, Head of US Clinical Operations, and is based in...Work at office
$169.22k - $253k
The Associate Director, Risk Based Quality Management is responsible for developing, implementing and optimizing... ...design and risk assessment to study conduct oversight and closeout.... ...trends, quality signals, and potential compliance issues from a portfolio perspective....Contract workTemporary workWork at officeLocal areaFlexible hours- ...Time Recruitment Solutions (RTRS) Hiring: Quality Manager - Specialized Manufacturing We’... ...maintain high standards of quality and compliance. Investigate and resolve product non-conformities... ...$199,400.00 4 days ago Sr Mgr/Associate Director, GMP Quality Assurance Wilmington, MA $6...16 hoursFull time
$229k - $280k
...conditions. What You’ll Do The Senior Director, Quality Systems is a high-impact leadership... ...deviation closures without compromising compliance. Build and mentor a high-performing team... ...clinical trials to late-stage pivotal studies. Deep knowledge of global GxP...Full timeLocal areaFlexible hours3 days per week- ...operations. Nanobiosym is looking for a Quality Manager for its High-Complexity Testing... ...Quality Manager will provide quality and compliance oversight to the Nanobiosym diagnostic... ...associated regulations, and support the Lab Director and leadership in maintaining audit...Immediate start
- Vertex Pharmaceuticals Inc is seeking an Operational Area Quality Senior Manager to provide quality leadership for assembly manufacturing... ..., CAPAs, change controls, supplier quality, and regulatory compliance. You will partner with manufacturing, engineering, supply...
- A biomedical technology company in Cambridge, MA is seeking a Quality Manager to oversee compliance and quality management in its CLIA laboratory. The ideal candidate will have a Bachelor of Science degree and a minimum of 8 years’ experience in the FDA regulated industry...
$215k - $260k
Job Summary The Senior Director, U.S. Quality is responsible for leading and executing the Quality Management strategy across the U.S. business, ensuring compliance, operational excellence, and continuous improvement across all quality systems, processes, and products....Temporary work$226.8k - $306.8k
...a strategic and technology‑savvy leader to serve as Senior Director, Quality Technology, responsible for advancing digital capabilities across... ...that support Quality Management System (QMS) processes, compliance, and operational excellence across GxP environments. The Senior...Full timeTemporary workLocal areaFlexible hours- eternalHealth, a Boston-based start-up transforming Medicare Advantage, seeks a Director of Quality to design, implement, and continuously improve the Quality Management Program. You will ensure CMS regulations, accreditation standards, and DOI requirements are met while...
- Verastem Oncology is seeking a Quality Assurance professional to oversee quality systems and ensure regulatory compliance for its biopharmaceutical operations. The role involves leading quality initiatives, maintaining relationships with technical teams, and ensuring adherence...
$180.8k - $271.2k
Job Description General/Position Summary The Director of Analytical Product Quality is responsible for the quality oversight of analytical development... ...the QA oversight of the stability program to assure compliance with internal Vertex procedures and EU/US regulatory standards...Contract workSummer workFlexible hours- A biotechnology organization is seeking an Associate Director, Global Quality to oversee global quality compliance across R&D. This role involves leading compliance projects, ensuring inspection readiness, and embedding quality processes. Candidates should have a strong...
- Vertex Pharmaceuticals seeks a Director of Analytical Product Quality in Boston. This role involves quality oversight in analytical development for Cell & Gene therapies, ensuring compliance with internal procedures and regulatory standards. The ideal candidate will have...
$238.3k - $327.66k
...pathways across key markets (US, EU, etc.) and leading the Quality organization ensuring compliance with all applicable regulations. Develop and execute... ...in strategic business decisions, including clinical study design and regulatory approvals. Drive global regulatory...Temporary workLocal area- Quality Control Manager (QCM), Federal Construction Location & Employment Type Columbus, GA Full-Time, Onsite, Federal Project Assignment... ...and manage submittals, RFIs, and quality documentation for compliance with contract specifications Perform daily quality control...Hourly payDaily paidFull timeContract workFor contractorsFor subcontractor
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