Senior Clinical QA Leader - GCP, Audits & CAPAs
$148.5k - $203kQualStaff Resources
QualStaff Resources is seeking a Sr. Clinical QA Manager in San Diego, CA. The ideal candidate will have 6-8 years of experience in Clinical Quality Assurance and will lead efforts in risk mitigation, GCP compliance, and quality systems. This onsite position offers a salary range of $148,500 - $203,000 annually. Responsibilities include overseeing clinical QA, preparing for inspections, and ensuring compliant study conduct. Join a diverse and equal opportunity employer focused on advancing clinical quality. #J-18808-Ljbffr
- ...Neurocrine Biosciences in San Diego seeks a Sr. Clinical QA Manager to lead Clinical Quality Assurance efforts across various projects. This role requires expertise in GCP audit management, compliance with FDA regulations, and strong leadership skills. Ideal candidates...Senior
$112k - $153k
...company in San Diego is seeking a QA Manager responsible for ensuring quality oversight in GCP activities. The ideal candidate... ...least 5 years of experience in Clinical Quality Assurance and a strong understanding... .... This role includes managing audits, preparing status reports, and...Suggested$120k - $150k
UNAVAILABLE is seeking a Senior QS Specialist II in San Diego, California, responsible for... ...position demands extensive experience in QA within GMP regulated environments, focusing... ...leadership skills, with a strong background in audit management and training coordination. The...Senior$158.1k - $216k
...Neurocrine Biosciences, a leading biopharmaceutical company in San Diego, is seeking a Sr. Principal Specialist in Clinical Database Programming to provide strategic leadership for the clinical database programming function. The role requires extensive experience in database...SeniorFull timeContract work$133k - $166k
...Senior Manager, Quality Assurance GCP page is loaded## Senior Manager, Quality... ...robust preclinical and clinical development pipeline... ...Quality Assurance (QA) function, and... ...and oversee assigned audits, support regulatory... ...trend audit findings / CAPAs / resolution processes...SeniorLocal area$90k - $110k
...System and ensure compliance with GMP, FDA, and ISO standards. This temporary position will assist with key quality activities such as CAPA processes, deviation management, and training programs. The ideal candidate will have a minimum of five years of relevant experience...SeniorTemporary work$148.5k - $203k
...Sr. Clinical QA Manager - Pharmaceutical Industry QUICK FACTS Location... ..., ICH guidelines, and GCP standards ~ Experience with clinical trial audits, vendor audits, and investigator... ...needed. Guide remediation and CAPA development to ensure compliant...SeniorPermanent employmentLocal area- Neurocrine Biosciences in San Diego, California is seeking a Clinical Data Management Lead to provide strategic oversight of clinical data management activities across programs. Candidates should possess extensive experience in managing clinical data, ensuring high-quality...Senior
- ...Crystalys Therapeutics is looking for a Clinical Trial Manager/Sr. Clinical Trial Manager in San Diego to ensure exceptional clinical trial planning and execution. The role involves leadership in clinical operations and cross-functional activities, supporting numerous...SeniorWork at office2 days per week
$148.5k - $203k
...Sr. Clinical QA Manager page is loaded## Sr. Clinical QA Managerremote type: On-Sitelocations... ...limited to):Good Clinical Practice (“GCP”) Audit Management:* Lead, plan, conduct, and oversee... ...(e.g., audit observations, deviations, CAPAs, GCP QA activities) for management...Senior$112k - $153k
...biopharmaceutical company in San Diego is seeking a QA Manager for oversight of GCP activities. The ideal candidate will have... ...and at least 5 years of experience in Clinical Quality Assurance. Responsibilities include managing GCP audits, approving deviations, and preparing...$95.9k - $159.9k
...Sr Clinical Research Associate job at Dexcom, Inc.. San Diego, CA. The... ...DXCM) is a pioneer and global leader in continuous glucose... ...processes, on-time monitoring, audit-readiness both at sponsor and... ...functionally to achieve goals. Strong GCP and clinical study background,...SeniorRemote workWorldwideHome officeFlexible hours- A healthcare technology company is seeking a Senior QA Engineer to enhance their automated testing framework. This remote role involves collaborating with product and engineering teams, mentoring peers, and ensuring high-quality product delivery. Candidates should have...SeniorRemote work
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$110.8k - $151k
...in San Diego seeks a Statistical Programmer with experience in the biopharmaceutical industry. This role focuses on deadlines for clinical data evaluation and SAS programming. The ideal candidate has a BS/BA degree, 4+ years of experience in statistical programming, and...Senior- Sharp HealthCare is seeking a qualified Clinical Laboratory Scientist (CLS) in San Diego, California. The ideal candidate will hold a valid California CLS license and have experience in a clinical laboratory setting. This position involves providing technical expertise...
- ...preferably including public accounting. This role offers opportunities to enhance reporting efficiency and contribute to financial audits while fostering a collaborative work environment. Compensation includes competitive packages and comprehensive benefits. #J-18808-...Senior
- ...them most. The Senior Director of... ...supporting Capricor’s clinical-stage and... ...senior Quality leader and strategic advisor... .../Investigations/CAPA, Training and Qualification... ...PAIs), partner audits, and health... ..., including GCP compliance and... ...high-performing QA and Quality Systems...SeniorWork at office
- ...Description Job Summary: The Clinical Trial Manager/Senior Clinical Trial Manager will... ...requirements, ICH/GCP guidelines, and internal SOPs... ...the resolution of applicable audit findings. Ensure audit-ready... ...management through resolution (e.g. CAPA) of any site or study level...SeniorContract workLocal area
$100k - $125k
...Arrowhead Pharmaceuticals in San Diego, CA is seeking a Clinical Research Associate (CRA) to support the Clinical Operations Manager. This... ...and ensuring compliance with clinical protocols and ICH-GCP guidelines. The ideal candidate will have at least 5 years of clinical...Senior- ...in San Diego is seeking a Study Physician to oversee medical operations for clinical trials. You will guide the clinical team and ensure adherence to protocols and Good Clinical Practices (GCP). A minimum of 3 years in medical monitoring and an MD or equivalent is required...Senior
- Arrowhead Pharmaceuticals is seeking a Supply Chain Manager for clinical studies in San Diego. The role focuses on ensuring uninterrupted... ...functional teams, and ensuring compliance with standards like GMP and GCP. The ideal candidate has 6-8 years of experience in clinical...Senior
$85.12k - $95.76k
...seeks a Sr. Compliance Specialist to ensure adherence to regulatory standards within the organization. This role involves leading audits and inspections, contributing to a culture of compliance, and supporting Quality Management Systems. Ideal candidates will have a Bachelor...Senior$85k - $121.8k
...Encore Capital Group in San Diego, CA is seeking a Senior GRC Analyst to manage IT compliance, risk management, and data governance roles... ...IT policies, assessing risks, and supporting compliance audits. The ideal candidate will hold a Master's degree and possess certifications...Senior- ...in a healthcare setting. Responsibilities include application support, leading initiatives, and ensuring effective communication. Candidates must demonstrate strong leadership skills and a thorough understanding of clinical and operational workflows. #J-18808-Ljbffr...Senior
- Intuit Inc. is seeking a Lead, SOX Program Strategy & Audit Excellence in San Diego who will serve as the primary liaison to the Technology organization. This role is pivotal for managing IT General Controls and operationalizing the AI SOX Governance Framework. The ideal...Senior
$120k - $170k
...molecules and biologics. Arrowhead is leading the field in bringing the promise of RNAi to address diseases outside of the liver, and our clinical pipeline includes disease targets in the liver and lung with a promising pipeline of preclinical candidates. Arrowhead's...Senior- Werfen is seeking a Senior Quality Systems Specialist II in San Diego, California, responsible for leading the Quality Management System (QMS) processes to comply with regulatory standards such as GMP, FDA, and ISO. This role involves managing key quality processes, mentoring...Senior
$270k - $320k
...ORIC Pharmaceuticals is a clinical stage biopharmaceutical company... ...serve as a Medical Director or Senior Medical Director at ORIC Pharmaceuticals... ...investigators, key opinion leaders, advisory boards, and... ...regulatory requirements (FDA, EMA, ICH/GCP) ~ Familiarity with current...Senior$120k - $140k
...quality standards in supplier quality management. This role includes developing a comprehensive supplier quality program, managing audits, and ensuring compliance with GMP standards. The ideal candidate should have a Bachelor’s degree in Biological Science and over 7 years...Senior
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