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Applicants seeking the rank of Assistant Clinical Professor should demonstrate a track record or promise in teaching and research. Engaging in research and service as defined in the college's Clinical Non-Tenure Track Faculty Manual.
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The MSL may have contact with internal colleagues in pharmaceuticals, marketing, sales, research and development, strategy/portfolio management, regulatory, and medical affairs team members.
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This new joint venture will establish a fully integrated oncology research organization aimed at expanding clinical research, accelerating drug development and increasing availability and access to clinical trials for community oncology providers and patients, including those in underserved communities.
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In addition, through the combination of their clinical research networks, data and analytic capabilities and more, the joint venture will bring greater efficiency to the drug development process – making it possible to help more cancer patients access new, life-saving medications.
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Counsel internal clients on a variety of regulations and policy initiatives, including the FDA, Stark, open-payments, anti-kickback, anti-bribery, fraud and abuse, HITECH and HIPAA.Independently negotiate, document and close speaker, clinical research and clinical trial agreements.
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Patient voice) that are effective, streamlined and are by design initiated at the optimal time in the clinical drug development process-Ensure GCO diversity related roles and responsibilities within external partners (e.g. CROs, specialty Vendors) are well defined, clear and aligned to goals set by related internal groups (e.g. patient advocacy, ID Office, field medical, regulatory affairs, etc.
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The Clinical Trials Regulatory Specialist I is an entry-level position supporting regulatory affairs in clinical trial research. Knowledge of clinical research practices.
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Supports processes and monitors practices to ensure regulatory documentation involving clinical trials complies with Institutional Review Board (IRB) policies and procedures and regulations. Assists regulatory team (Regulatory Specialist II and III) in research efforts by facilitating the protocol approval process and maintaining documentation of regulatory compliance throughout the trial's duration for research studies involving human subjects.
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Establishes and maintains ongoing cooperative and productive relationships with appropriate internal and external contacts, including government granting agency contacts (in coordination with Government Affairs) and research administration contacts at Emory, Georgia Tech, and other academic partners.
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Offering expert guidance from concept-through-commercialization, including product design and engineering, preclinical and clinical development, data management, market access, regulatory affairs and quality assurance, Veranex enables accelerated speed to market, controlled development costs, development risk mitigation, and accelerated market viability assessment.
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This individual will leverage their deep subject matter expertise in HEOR ( economics, epidemiology, statistics, and health services/clinical research) to teach colleagues how to design and deliver compelling HEOR evidence that improves lives and advances UCB’s strategy.
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The Clinical Research Associate (CRA) will support successful and timely start-up and completion of clinical trials and be a key member of the Organization of Chief Medical Officer (OCMO) Global Clinical Affairs team.
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The Chief Operating Officer is an executive leadership position that assumes line responsibility and authority for the administrative direction, evaluation, and coordination of the functions and clinical operations of the full continuum of care of a 152-bed inpatient specialty hospital for persons with spinal cord injury, brain injury and other neurological disorders.
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Working in conjunction with the medical affairs and clinical development teams, evaluate potential external clinical research collaboration opportunities and facilitate the conduct of external clinical investigator-initiated trials (IITs) and company-sponsored trials.
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