Associate Director, Clinical QA & GxP Compliance
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Ultragenyx Pharmaceutical is seeking an Associate Director of Quality Assurance who will lead the creation and evolution of QA strategies, aligning with global regulations and health authority requirements. The role partners with senior leadership to strengthen inspection readiness and drive enterprise quality improvements. The position requires proven experience in audits, regulatory inspections, and cross-functional collaboration, with a strong focus on compliance, risk mitigation, and process #J-18808-Ljbffr Storyboard
$199.2k - $246.1k
.... Position Summary The CQA Associate Director provides strategic leadership... ...and model a culture of compliance and quality excellence across... ...compliances and risk areas across clinical programs and drive... ...and strategic direction to QA personnel, SMEs, and contract...SuggestedFull timeContract workWork at officeLocal areaFlexible hoursShift work2 days per week3 days per week- Olema Oncology is seeking an Associate Director, GMP Quality to oversee GMP activities for clinical and commercial products, including... ...of batch records and supplier compliance. The role requires... ...background in FDA-regulated GMP QA, NDA/BLA submissions, and quality...Suggested
$186k - $220k
...and peptide drugs. We are advancing a clinical‐stage pipeline of differentiated treatments... ...location.Position Summary:The Associate Director of Clinical Operations plays a pivotal... ...phases, ensuring efficient execution and compliance with regulatory standards. This senior...SuggestedContract workRemote work$215.54k - $260.82k
Associate Director, Clinical Regulatory page is loaded## Associate Director, Clinical Regulatorylocations: South San Franciscotime type: Full timeposted... ..., adherence to company policies, maintains training compliance and provides ongoing feedback on growth, development and...SuggestedWork experience placementLocal area- ...talent, we are open to remote.As an Associate Director, Quality Assurance Compliance at Gilead you will have the... ...inspection metrics dashboards) in a GxP‑compliant and inspection‑defensible... ...knowledgeable and credible resource for QA compliance in other departmentsIn-depth...SuggestedFull timeFor contractorsWork at officeLocal areaRemote work
- Initial Therapeutics, Inc. is seeking an Associate Director, Quality Management Systems (QMS) in South San Francisco. This role involves leading... ...QMS function, implementing quality policies, and ensuring compliance with regulatory standards in the development of new cancer...
$167.5k - $246.5k
Vir Biotechnology, Inc. is a clinical-stage biopharmaceutical company focused on powering... ...Biotechnology is looking for an Associate Director, Clinical Transactional Counsel to manage... ...development agreements to ensure compliance with country regulations, align with business...Full timeContract workWork at officeLocal areaWork visa3 days per week$176.5k - $246.5k
...Vir Biotechnology, Inc. is a clinical-stage biopharmaceutical company focused on powering... ...OPPORTUNITYVir Bio is looking for an Associate Director, Clinical Operations, responsible for... ...the overall site management ensuring compliance with Good Clinical Practices (GCP) and...Full timeWork at officeWork visa3 days per week- ...Job Description Job Description Job: Associate Director, Clinical Operations (Late-Phase) Location: Thousand Oaks, CA or San Francisco,... ...trial oversight. Ensure clinical studies are conducted in compliance with SOPs, ICH/GCP guidelines, and FDA regulations....Full timeFor contractorsLocal area
$160k - $180k
...The Associate Director, IT Compliance is responsible for organising, leading and continuously... ...compliance guidance for GxP computerised systems. This... ...regulated industry such as clinical research, pharmaceutical,... ...stakeholders across IT, QA, Legal, Privacy, Information...Full timeContract workWorldwideFlexible hours- A leading life sciences company in South San Francisco is seeking a Director of Clinical Quality Assurance to ensure compliance with FDA regulations and oversee GCP QA programs. The ideal candidate will have extensive experience in clinical quality assurance and expertise...
$190k - $240k
...us to make a real difference, every day. Position Title Associate Director, Clinical Scientist Reports To: VP, Clinical Development Lead (CDL)... ...and/or identifies critical risks and mitigations Maintains compliance in accordance with FDA, EMEA, ICH and GCP guidelines as...Flexible hours$230k - $240k
...breakthroughs.Position Description:Calico is seeking an Associate Director, Medical Writing to provide leadership and... ...leading the review/approval process of high quality clinical and regulatory documents, in compliance with applicable guidelines and regulations. The successful...Work at office$190k - $240k
Join to apply for the Director of Clinical Quality Assurance role at BioSpace... ...across Alumis. The Clinical QA Director is responsible to... ...ongoing clinical programs are in compliance with applicable health... ...0.00-$220,000.00 3 days ago Associate Director, GMP Quality Assurance...Full time$190k - $280k
...extracellular protein degraders into the clinic. Lycia is headquartered in South San... .... Lycia Therapeutics is seeking a Director or Associate Director of Clinical Science who will... ...and CRA/staff training Ensure compliance with ICH-GCP guidelines, regulatory requirements...Work at officeFlexible hours2 days per week3 days per week$200.7k - $234.15k
...Associate Director, Regulatory Affairs Cytokinetics is a specialty cardiovascular biopharmaceutical... ...serve as regulatory lead for assigned clinical studies Identify potential... ...EMA, ICH), including an understanding of GXP ~ Experience supporting regulatory submissions...$155k - $185k
...Associate Director, EH&S and Facilities Sutro is seeking an Associate Director, EH&S and Facilities to lead EH&S compliance and equipment service management at our South San Francisco headquarters. Responsibilities Develop and partner with external consultants to lead...Local area$195.39k - $227.96k
...Associate Director, Clinical Supply ChainCytokinetics is a specialty cardiovascular biopharmaceutical company, building on its over 25 years of... ...across the organization, as well as maintaining regulatory compliance to meet corporate objectives.Key ResponsibilitiesSupply...Worldwide$144k - $240k
...focused on transforming the lives of patients with severe immune-mediated diseases by developing novel targeted therapies with outsized clinical impact, faster. To accomplish this, we are seeking top talent to join us on our journey.As the Lead, Clinical Pharmacology,...Temporary workLocal area$190k - $230k
...Posted: 2026-07-18Position SummaryReporting to the Senior Director of Medical Affairs, this position will be responsible... ...functionally with leaders and teams across Medical Affairs, Compliance, IT, Finance, Clinical Development, and Legal. Strong collaboration skills and...Work at officeRemote workFlexible hours- Kardigan is seeking an Associate Director, Clinical Scientist to lead analysis and monitoring of study data across cardiovascular programs, guiding phase 2B and phase 3 trials, reporting to the VP CDL and collaborating with governance teams. The ideal candidate has 5+...
$120.2k - $223.2k
...in the Global Legal Pharma Department.Associate Program Directors of Commercial Medical Legal... ...proactively identifying and addressing compliance issues.Effectively integrate regulatory... .../pharma industry (compliance, legal, clinical affairs, regulatory and product marketing...Full timeWork experience placementLocal areaWorldwideRelocation package$166k - $209k
...and peptide drugs. We are advancing a clinical‐stage pipeline of differentiated treatments... ..., continuous improvement, and compliance of Structure Therapeutics' GxP-regulated applications. Reporting to the Associate Director, GxP Operations, this role is the primary...Contract workWork at officeRemote work$198k - $257k
...long-term strategic partner for global clinical development. Our unique business model... ...Primary Function: The Associate Director, Regulatory Affairs supports the development... ...alignment with regulatory expectations. Compliance: Execute regulatory activities in compliance...Full timeWork at officeWorldwideRelocation package- Vera Therapeutics Inc. in Brisbane, CA is seeking an Associate Director, Drug Substance Manufacturing - Upstream Process. You will oversee all... ...sections for NDA/BLA submissions and coordinate with CMOs and QA/regulatory teams. The role requires strong leadership, cross-functional...
$175k - $210k
Associate Director, Drug Substance Manufacturing - Upstream Process Brisbane... ...of BAFF and APRIL may prove clinically meaningful. Vera... ...such as project management, QA and Regulatory, the ideal candidate... ...Office of Federal Contract Compliance Programs (OFCCP) website at...Contract workFor contractorsFor subcontractorWork at officeFlexible hours- ...week onsite in San Mateo County Associate Director of Quality Systems We are working with a clinical stage biotech focused on... ...a focus on Veeva systems and GxP compliance. The ideal candidate will lead... ...weeks ago Executive Director GMP QA (Good Manufacturing Practice Quality...Full time3 days per week
- ...a talented and highly motivated Associate Director, Quality Management Systems (QMS)... ...systems, and risk assessment in compliance with internal and external clinical, safety, quality, and regulatory... ...control activities comply with current GxP guidelines. Implement continuous...Temporary workFor contractors
$80 - $93 per hour
Job Title : Associate Director, Quality Location : Hybrid Reports to : Vice... ...System (QMS), and ensuring compliance with FDA, ICH, and other regulatory... ...ensures compliance with GxP regulations (GLP, GMP, GCP... ...preclinical research through clinical development in a fast-paced,...Hourly payFull timeTemporary workPart time$174k - $203k
...Mission to Protect Humankind!Vaxcyte is a clinical-stage vaccine innovation company... ...communications and decision making.Summary:The Associate Director, Process Validation and Risk... ...support commercial readiness, regulatory compliance, and lifecycle management.The incumbent...
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