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The Global Genomics team within Translational Medicine function leverages Next Generation Sequencing (NGS) and other advanced technologies to match the right patient to the right drug and support precision oncology approaches for the AZ Oncology pipeline.
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Minimum of 5 years' experience as an operations and/or analytics contributor, with a proven track record of leading data-driven strategy design and implementation. Manage the commercial data warehouse requirements and master data management plan for timely, complete, and accurate reporting and analytics.
$194,856 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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The company facilitates affordable, non-exclusive access to the entire drug discovery community from academic scientists, small and medium biotech, to the largest biopharma. You will support with systems administration and maintenance (JazzHR, Radford Aon, AccrueCMS, Lattice, and TriNet), ensuring data integrity and accuracy and support with pulling reports.
Full-timeExpandApply NowActive JobUpdated 22 days ago - UpvoteDownvoteShare Job
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The Director, Pharmacovigilance & Risk Management will lead effective pharmacovigilance operations both internally and through a third-party Pharmacovigilance vendor related to the processing of adverse events from clinical trials and postmarketing surveillance in support of US market launch of a newly approved drug product.
Full-timeExpandApply NowActive JobUpdated 17 days ago - UpvoteDownvoteShare Job
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Nuvalent is an exciting early-stage company, bringing together experienced scientists and industry veterans with a proven track record in drug discovery, oncology drug development, and company building.
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Own’s operational excellence – design, implement and monitor for Drug Discovery Units and Research line functions through (i) IT, (ii) Finance/Legal, (iii) Procurement, and (iv) Quality, Data Privacy.
$322,300 a yearFull-timeExpandApply NowActive JobUpdated 22 days ago - UpvoteDownvoteShare Job
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Provide Trial Operations leadership across multiple studies to support the design, development, execution, and delivery of clinical programs in accordance with Clinical Development Plans and timelines for assigned program area; closely collaborate with Clinical Development, Biostatistics, Data Management, Regulatory, Medical Writing, Medical Affairs, Supply Chain, and Development Program Management to ensure highly integrated cross functional project plans for programs and trials.
$233,500 a yearFull-timeExpandApply NowActive JobUpdated 22 days ago - UpvoteDownvoteShare Job
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In collaboration with the Clinical Study Lead, Program level clinical operations leadership, and CRO (if applicable), ensure procedures and support are available to facilitate delivery of high-quality clinical data.
Full-timeExpandApply NowActive JobUpdated 22 days ago - UpvoteDownvoteShare Job
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Reporting into the Head of Research Strategy and Operations, an individual in this role integrates budget, contracting, purchasing, and resourcing data and information from across the business to create an overall holistic view of Research operational health.
Full-timeExpandApply NowActive JobUpdated 19 days ago - UpvoteDownvoteShare Job
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Contribute to the preparation and review of clinical study documents including the Investigator Brochure, Investigational New Drug Applications (IND), study protocols, clinical study reports, applicable sections of New Drug Applications (NDA) and or Marketing Authorization Application (MAA), updates to the IND, NDA and other safety reports.
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Oversee the collection, analysis and interpretation of clinical trial data, working closely with Clinical Development, Biostatistics and Data Management teams to ensure data accuracy and integrity.
Full-timeExpandApply NowActive JobUpdated 13 days ago - UpvoteDownvoteShare Job
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With an in-house technology platform built from scratch, we have rapidly generated multiple drug discovery programs that are advancing towards the clinic. Delivers crisp execution from planning to close-out to ensure adherence to timelines and goals while maintaining quality in accordance with FDA, EMEA, GCP, and ICH guidelines to deliver regulatory-grade data and outputs on time and within budget.
Full-timeExpandApply NowActive JobUpdated 22 days ago - UpvoteDownvoteShare Job
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Manage strategic study operations including: study sites and tracking systems for regulatory submissions, CRO KPIs, drug supply and use, enrollment of subjects, regulatory document flow, study timelines, all budgetary and financial information, Pharmacovigilance/Serious Adverse Events, performance metrics, data flow, etc.
Full-timeExpandApply NowActive JobUpdated 22 days ago - UpvoteDownvoteShare Job
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The Director, Clinical Operations is a leadership role responsible for overseeing and managing all aspects of clinical operations for a high priority immunology program. 10+ years of experience in clinical operations within the pharmaceutical or biotechnology industry.
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This individual possesses clinical operations expertise with a track record of success, working with peers and stakeholders across multiple disciplines to drive programs with multiple studies and indications through all phases of clinical trials (Phase I-III.
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data drug jobs Title: operations in Boston, MA
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