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Manages clinical trial studies for the Department of Medical and Molecular Genetics which includes direct oversight of all physicians, genetic counselors, dietitians, and clinical research staff involved with the study.
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The purpose of the Clinical Design Scientist is to provide Medical and scientific leadership in the clinical program and trial design of assets approaching and/or primarily in Phases II to IV. In order to accomplish this, the Clinical Design Scientist must have a deep understanding of the biopharmaceutical industry, drug development process, the therapeutic area that is relevant for the programs in development, clinical research, and clinical program and study design.
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Provides various other clinical research study or project support as needed (such as assisting with budget development, invoicing for adverse events, billing compliance and patient billing resolution.
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The purpose of the Clinical Design Physician is to provide Medical and scientific leadership in the clinical program and trial design of assets approaching and/or primarily in Phases II to IV. In order to accomplish this, the Clinical Design Physician must have a deep understanding of the biopharmaceutical industry, drug development process, the therapeutic area that is relevant for the programs in development, clinical research, and clinical program and study design.
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Must have a deep understanding of the biopharmaceutical industry, drug development process, the therapeutic area that is relevant for the programs in development, clinical research, and clinical program and study design.
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Our center has more than 50 clinical research projects involving bleeding disorders, sickle cell disease, thrombosis and more. What You Will Do As a Research Coordinator, you will be responsible for executing research projects under the direction of the primary investigator and for performing in accordance to study regulatory processes, standard operating procedures, and study protocols.
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If you are dedicated to advancing your knowledge and clinical expertise through research and professional discourse, we would like to meet with you to share our mission, vision, and values for the post-acute industry.
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The clinical research nurse achieves this by coordinating regulatory aspects of clinical trials, collaborating with team members and key stake holders both within and outside of IU Health, screening and enrolling patients in clinical trials and carrying out study visits.
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Collaborate and complement clinical research staff in the design and conduct of clinical trials (e.g. sample size, patient commitment, timelines, grants, and governance review interactions.
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Long-Term OpportunityCompetitive PayRequirements:Experience using Epic EMRClinical Research experience HIGHLY preferredExperience with medical terminology REQUIREDResponsibilities:Reads, comprehends, and follows complex study protocols for a variety of clinical research studies (early and late phase.
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Some studies such as clinical trial in-person focus groups pay as high as $500 per study. This opportunity is for completing market research opportunities with independent brands via online or phone.
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Knowledge of study design and outcomes research methods. Humana's Clinical Analytics Team is seeking a Research Scientist (Remote). Our team identifies opportunities and builds solutions to improve clinical outcomes and lower costs for millions of Medicare Advantage beneficiaries through an evidence-based approach using data analytics, clinical expertise, strategic mindset, and rigorous study designs.
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Be aware of current trends and projections for clinical research, practice, and access in the therapeutic area(s) relevant to the product. Clinical Research/Trial Packages, Execution and Support.
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Must be certified within three (3) years from hire by (Certified Clinical Research Associate (CCRA - ACRP), Certified Clinical Research Coordinator (CCRC-ACRP) Required. 5+ years: Requires one (1) of the following: 1) Bachelors degree or associate degree and a minimum of five (5) years clinical research experience OR equivalent combination of relevant education and/or experience.
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WHAT YOU CAN EXPECT Conduct clinical trials that involve human subjects according to written protocols and departmental standards while adhering to Good Clinical Practice (GCP) Guidelines.
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study clinical research jobs in Indianapolis, IN
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