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Build and lead capability to oversee observational study documentation including regulatory system management, trial master file, clinical trial management system (as needed) with almost no direct supervision.
$221,170 - $286,220 a yearFull-timeExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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Master's degree in Computer Science, Engineering, Business Administration, or related area and 4 years' experience as a product manager, ideally working on consumer-facing, large-scale, highly complex B2B/C products, We value candidates with a background in creating inclusive digital experiences, demonstrating knowledge in implementing Web Content Accessibility Guidelines (WCAG) 2.2 AA standards, assistive technologies, and integrating digital accessibility seamlessly.
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Responsible for filing necessary documents in the electronic trial master file (eTMF), and supporting regular cross-functional reviews of the eTMF. We are seeking a talented and experienced Clinical Trial Management Associate to work hybrid or remotely based in our South San Francisco office.
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Expert in configuration of SAP IBP including Master Data, Planning Area, Key Figure, Key Figure Calculation and Miscellaneous Settings Demand, Supply for Optimizer/Heuristic. Expert in configuration of SAP IBP including Master Data, Planning Area, Key Figure, Key Figure Calculation and Miscellaneous Settings Demand, Supply for Optimizer/Heuristic.
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Knowledge of electronic trial master file (eTMF) systems and document management processes. The Senior Clinical Research Associate I (CLRA) is responsible for site management deliverables on assigned protocols and may act as a lead CRA for the study, providing guidance and support to other CRAs on the team.
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The Digital Pathology Principal Scientist will be accountable for implementation of digital pathology including image analysis and artificial intelligence/machine learning (AI/ML) algorithms for clinical trial biomarkers including pharmacodynamic, mechanism of resistance, patient selection and biomarker discovery.
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BA or BS and 12+ years' experience in compliance and trial master file in pharmaceutical/biotechnology industry. The Associate Director, Clinical Records & Information Management will partner with cross functional teams as well as Clinical Research Organization (CRO and Functional Service Provider (FSP) to ensure timely and quality delivery of the TMF. This role is a member of the Clinical Records leadership team to ensure optimum implementation of the TMF technical capabilities and oversight of standardization, training, quality, and timely clinical trial documentation across the clinical program.
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Complete trial-specific Statement of Work (SoW) based on parameters supplied by Master Service Agreement (MSA) for Electronic Data Capture (EDC), electronic Patient Reported Outcomes (ePRO) and Interactive.
Full-timeRemoteExpandApply NowActive JobUpdated 10 days ago - UpvoteDownvoteShare Job
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CARGO is currently evaluating its lead program, CRG-022, an autologous CD22 chimeric antigen receptor (CAR) T-cell therapy candidate, in a potentially pivotal Phase 2 clinical trial in patients with large B-cell lymphoma (LBCL) whose disease relapsed or was refractory (R/R) to CD19 CAR T-cell therapy.
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Participate in technology-transfer activities with internal and external partners to support early‑stage clinical programs. CARGO Therapeutics, Inc. is a clinical-stage biotechnology company positioned to advance next generation, potentially curative cell therapies for cancer patients.
$100,000 - $138,000 a yearFull-timeExpandApply NowActive JobUpdated 3 days ago - UpvoteDownvoteShare Job
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Housed there are our program offices for 4-H, Agriculture, Urban Forestry, the Master Food Preserver, Master Gardener, and Nutrition Education Programs. Housed there are our program offices for 4-H, Agriculture, Urban Forestry, the Master Food Preserver, Master Gardener, and Nutrition Education Programs.
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Reporting to the Associate Director of Facilities Management and Planning, the Sr. Manager of Space an Logistics is a department manager responsible for space at SLAC. This includes development of space standards/policy, space master planning, and site master planning with collaboration with Stanford University in collaboration with the Lab’s Director’s Office, SLAC’s Office of Strategic Planning, and SLAC Campus Planning.
$142,000 - $194,000 a yearFull-timeExpandApply NowActive JobUpdated 3 days ago - UpvoteDownvoteShare Job
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We currently have an exciting opportunity for a highly motivated research associate to join our protein purification and QC group within the Protein Therapeutics Department. Title : Research Associate - Protein Therapeutics.
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Technical Development Research Associate IILocation: South San Francisco, CADuration: monthsDescription:Job Knowledge & ScopeClient , in the Cell Culture and Bioprocess Operations department, is responsible for providing support to pre-Early Stage Research to Early Development projects with high-throughput protein production from mammalian transient cultures.
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This team aims to address these challenges and enable customers to benefit from Snowflake’s rich features and integrated platform capabilities while embracing their choice of open table standards (e.g., Apache Iceberg), file formats (e.g.,Apache Parquet), storage solutions, and third-party open source tool set (e.g.,Apache Spark.
$214,000 - $327,750 a yearFull-timeExpandApply NowActive JobUpdated Today
trial master file jobs Title: clinical research associate Company: Parexel in San Mateo, CA
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