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Whether you are in the discovery sciences, ensuring drug safety and efficacy or supporting clinical trials, you will apply cutting edge design and process development capabilities to accelerate and bring the best.
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The right applicant will have sufficient clinical research experience to serve as the site principal investigator of a NIDfunded Clinical Trials Network (CTN) study. The Clinical Director oversees aspects of the 60-bed inpatient psychiatric hospital and provides input and guidance to the unit’s and agency’s psychology, psychiatry, nursing, and other staff.
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CfOR gives evidence regarding the frequency and distribution of disease or the clinical burden of disease, the natural history or clinical course of disease, the design of clinical trials, cost and utilization patterns and the safety and efficiency of interventions.
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Provide programming expertise on one or more clinical trials in programming, documentation, validation and review of summary tables, data listings, and graphs for inclusion in clinical reports or presentations in collaboration with project statistician.
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The Clinical QA Manager will be responsible for the development, maintenance and oversight of the GCP activities related to clinical trials. Battery Bio harnesses Vial's unique 90% lower cost structure to produce more affordable drug development with efficient, streamlined clinical trials.
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Provides or oversees ongoing medical monitoring for clinical trials, including but not limited to assessment of eligibility criteria, toxicity management, and drug safety surveillance. Has thorough understanding of pharmaceutical regulatory requirements and impact on development and execution of clinical trials.
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Travel to APAC locations to support animal labs, clinical trials, and regulatory testing. The Senior System Integration Engineer, APAC will be responsible for systems integration activities through all phases of development of a complex medical robotic system.
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Experience overseeing biotech phase 1 clinical trials; experience with oncology programs is preferred. This leadership role requires strategic planning, effective management, and collaboration with cross-functional teams to ensure the successful execution of clinical trials and studies.
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Work closely with other functional areas within R&D (clinical operations, data management, biostatistics, clinical pharmacology, nonclinical) to facilitate the execution of clinical trials and ensure high standards of study conduct are met.
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Fortrea is actively seeking motivated problem-solvers and creative thinkers who share our passion for overcoming barriers in clinical trials. Stay informed about the latest trends and developments in the clinical research industry.
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Drive business growth by securing new opportunities in site-based, hybrid, and fully decentralized clinical trials. The Clinical Research Division at The IMA Group is a dynamic hub of expertise and innovation, dedicated to advancing healthcare through clinical trials and studies.
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This position is responsible for collecting, reviewing, maintaining, and archiving essential Regulatory documents for the Trial Master File (TMF) in accordance with Good Clinical Practice (GCP), E6 ICH Guidelines and other regulatory guidance documents, relevant regulations (e.g., 21 CFR Parts 312 and 314, EMA Clinical Trials Directives), and Standard Operating Procedures (SOPs) as appropriate.
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We have a robust pipeline of ADCS in clinical trials for both hematologic and solid tumor cancers. and be responsible for developing and executing the business plans for the top customer accounts in the geography and educating key stakeholders including treating physicians, pharmacy and C-suite as appropriate on the clinical profile and value proposition of ZYNLONTA. This person will leverage approved resources and work with the cross-functional ADC Therapeutics team to educate and support the customer to ensure a positive experience with ZYNLONTA.
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Has a thorough understanding of clinical trials design and reporting process, as well as regulatory reporting requirements including electronic data submissions. Successfully interacts within Clinical Data Science, with Clinical Development and Regulatory Affairs groups on a frequent basis.
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Identifying and executing collaboration opportunities between expert KOLs in Endocrinology / Genetics / Rheumatology / Hepatology & Neurology andd Alexion medical affairs and clinical development such as publications, investigator-initiated trials, regional advisory boards, training, and speaker development programs.
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clinical trials jobs in California, MO
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