Associate Director, GCP QA
Scorpion Therapeutics
Role Summary The Associate Director of GCP/GVP/GLP-QA is responsible for supporting Mirum’s clinical study programs as the GCP-QA representative on the study management team, overseeing GCP quality assurance activities and compliance with applicable regulatory requirements, and developing and implementing policies and procedures to ensure quality standards in line with regulatory and quality guidelines. Additionally, this role supports GVP and GLP QA operational activities to ensure data integrity and regulatory compliance. The position requires experience with global CROs and GCP Vendors and knowledge of global GCP regulations. Responsibilities Achieve established timelines for deliverables. QA Representative for assigned Mirum’s Program’s Clinical Study Management Teams. Manage/Support BIMO inspection readiness activities Support GCP/GCLP/GVP internal audits. Provide quality oversight for the GCP/GVP/GLP vendor activities, including internal/external deviations, CAPAs, change controls, and KPIs/KQIs. Support GCP, GCLP and GVP Vendor Management/Audit Program. Ad hoc audits may be requested. Assist with planning and supporting Clinical Site Management/Audit Program. Ad hoc site audits may be requested. Assist with and support regulatory agency inspections for the GCP and PV impacted functions. Provide GCP/GCLP/GVP Training as necessary Support Quality Management Team (QMT) by providing monthly/quarterly updates based on role and responsibilities Support process improvement of QA department, KPI/QPI tracking and oversight. Manage GCP/GVP/GLP consultant(s) as needed Qualifications Bachelor’s Degree in a scientific discipline. 10-12 years of experience in the pharmaceutical industry, including 5-10 years in GCP Quality and 5+ years supervising GCP Quality internal staff and/or external consultants. Knowledge and demonstrated experience in the applicable GCP regulations, FDA Regulations and Good Clinical Practices, EMA EudraLex Regulations, and ICH Guidelines. Strong verbal and written communication. Knowledge of basic GVP, GCLP and GLP regulations. #J-18808-Ljbffr
$193.64k - $224.27k
...delivering meaningful therapeutics to patients. Overview The Associate Director, GCP Clinical Quality will play a key role in ensuring the... ...SOPs, and the overall Quality Management System (QMS). Perform QA reviews of essential clinical trial documents and assist in...SuggestedLocal area$195.67k - $253.22k
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$185k - $195k
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$164k - $221k
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...levels of management Advanced knowledge in regulatory (FDA, EMA, Health Canada and ICH) guidelines Reports to: Executive Director, CMC Regulatory Location: San Carlos, CA / US Remote Work Arrangement: Remote Compensation: The compensation...Remote work$200k - $269.8k
...headquartered in Redwood City, California. To learn more, visit The Associate Medical Director/Medical Director, will act as a key participant in the... ...Ability to drive timelines while maintaining quality and GCP compliance Preferred Education and Experience: MD or...Full time$167k - $195k
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...and inspection readiness for Clinical Operations. The Associate Director, Connect Process supports process analysis and documentation... ...Pharmaceuticals for Human Use (ICH) guidelines and Good Clinical Practice (GCP) governing the conduct of clinical studies Fluency with...Full timeFor contractorsWork at officeLocal areaRemote workWorldwide$195.67k - $253.22k
...improving the lives of patients for generations to come. As the Associate Director, Biostatistics, you will provide strategic and operational... .... Knowledge of FDA and EMA regulations, ICH guidelines, GCP and familiarity with standard clinical procedures. Strong...Full timeFor contractorsLocal areaOverseasFlexible hours$254k - $290k
...Job Description Job Description Description The role: We are seeking a creative, accomplished Assoc. Director or Principal Machine Learning Scientist to advance the state of the art in ML-driven therapeutic antibody design. At BigHat Biosciences our full-stack...$174.7k - $218.4k
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$154.3k - $204.3k
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...of builders, innovators, and dreamers across a wide range of disciplines. We are seeking a visionary and execution‑oriented Associate Director, Affinity Reagent Development and Characterization , to serve as a leader and scientist driving the affinity reagent development...Full time$186k - $233k
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...Managers, CRA's and Clinical Trial Assistants. Responsible for ensuring that clinical studies are carried out and delivered according to GCP and company SOPs. Assists with the creation and implementation of policies. Works cross-functionally to ensure that the teams provide...Contract workWork at officeLocal area3 days per week$180k - $200k
...Associate Director/ Director, Supply Chain Management Synthekine is a Menlo Park, CA based biotechnology company focused on discovering and... ...Knowledge of current requirements for GLP, cGMP, and GCP is also required Experience with regulatory submissions...Work at officeLocal area
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