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The Clinical Trials Management Associate will work closely with Technical Operations to ensure drug product quality and delivery, Translational Sciences to ensure timely site biomarker sample collection and shipments, and support the clinical operations team with TMF filing and other duties as assigned.
$114,500 a yearFull-timeExpandApply NowActive JobUpdated 2 months ago - UpvoteDownvoteShare Job
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As such, you will provide scientific input into design & implementation of clinical trials, their delivery, clinical data review and data cleaning, interpretation of results, reporting successfully on time, and activities required for worldwide registration of the product ( clinical input to NDA/BLA.
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Help educate the retina community about Adverum’s clinical trials and gene therapy programs. Adverum’s core capabilities include clinical development, novel vector discovery, and in-house manufacturing expertise, specifically in scalable process development, assay development, and current Good Manufacturing Practices quality control.
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Strong understanding of IT systems and infrastructure supporting drug discovery, clinical trials, regulatory compliance, contracts, HR, and Finance. Oversee the development and maintenance of systems supporting clinical trials and data analysis.
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Provides ongoing medical monitoring for clinical trials, including but not limited to assessment of eligibility criteria, toxicity management, and drug safety surveillance. Understands drug development phases and the nature of associated clinical trials across phases.
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NCH is transforming into an Advanced Community Healthcare System(TM) and we’re proud to: Provide higher acuity care and Centers of Excellence; Offer Graduate Medical Education and fellowships; Have endowed chairs; Conduct research and participate in national clinical trials; and partner with other health market leaders, like Hospital for Special Surgery, Encompass, and ProScan.
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Innova Solutions is immediately hiring Manager Vendor OutsourcingPosition type: Fulltime – Contract Duration: 12 MonthsLocation: REMOTE As Manager Vendor Outsourcing, you will: Job Description: The R&D Sourcing and Contracting Associate will be responsible for assistance in the pre-clinical / research, clinical sourcing in support of Client’s global Phase I-IV clinical trials, and other ad hoc projects in the Vendor Outsourcing department.
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Clinical Operations plays a key role in ensuring all Gilead clinical trials are performed in accordance with applicable SOPs, company policies and regulatory guidelines to provide timely and high-quality clinical data that supports global registration and commercialization of Gilead’s products.
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The Sr. Manager will have the opportunity to provide category management, sourcing and contracting expertise in clinical outsourcing of global Phase 1b-Phase 3 clinical trials. Develops global clinical development vendor strategy for a program or therapeutic area with a focus on Cell Therapy.
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Yoh has an exciting, opportunity for a Sr. Clinical Trial Manager - Operations to join our rapidly growing client based in San Francisco Bay Area. Compensation: $131,000 - 188,000 DOELocation: San Francisco Bay Area - Hybrid Type: Direct Hire Position Title: Sr. Clinical Trial Manager, Clinical Operations Position Summary:The Sr. CTM will report directly to the Head of Clinical Operations and will be responsible for the operational implementation of one or more clinical trials.
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Understand the use and application of IVD assays in clinical trials Experience in GCP regulations and guidance, such as ICH E6 R2. Specifically, you will partner with Regulatory, Safety, Clinical Operations, and Device Manufacturing to set the quality management system strategy for R&D for medical devices.
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Clinical trials are performed in accordance with applicable SOPs, company policies and regulatory guidelines to provide timely and high-quality clinical data that supports global registration and commercialization of.
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By unlocking the information present in microbial cell-free DNA, we're helping doctors quickly solve their most challenging cases, providing industry partners with access to the microbial landscape to accelerate biomarker discovery and clinical trials, discover novel microbes, to ultimately reduce patient suffering worldwide.
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Experience with Statistical Analysis System (SAS®) software, R software, and familiarity with software tools for designing statistically optimized clinical trials. Utilize experience with Statistical Analysis System (SAS®) software, R software, & familiarity with software tools for designing statistically optimized clinical trials.
$181,500 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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The Director of Clinical Quality Assurance (CQA) is a hands-on position responsible for ensuring clinical trials adhere to applicable GCP regulations (e.g., FDA, ex-US, country-specific), ICH guidelines, Standard Operating Procedures (SOPs), and current industry standards and practices.
$230,000 a yearFull-timeExpandApply NowActive JobUpdated Today
clinical trials jobs in Burlingame, CA
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