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This position requires a deep understanding of pharmaceutical manufacturing principles, process engineering, and regulatory compliance. Knowledge of regulatory requirements and quality systems in the pharmaceutical industry.
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Assist the regulatory specialist in preparing for all local and Central Institutional Review Board (IRB) documentation through the IRB, including submissions, continuing reviews, amendments, modifications, and adverse event reporting and all regulatory documentation with pharmaceutical companies and clinical research organizations (CROs.
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Posted Job TitleVeeva Quality Assurance Specialist (Abramson Cancer Center)Job Profile TitleClinical Research Regulatory Specialist BJob Description SummaryThe Abramson Cancer Center (ACC) of the University of Pennsylvania is a world leader in developing and conducting innovative clinical trials for the prevention, diagnosis, and treatment of cancer.
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The Clinical Pharmacist Specialist for Abdominal Organ Transplant is responsible for the provision of pharmaceutical care to all abdominal organ transplant (liver, kidney, and pancreas) recipients.
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Juris Doctor (J.D.) degree from an accredited law school. A law firm in Philadelphia, PA, is seeking a Mid-level Intellectual Property Attorney with 4+ years of experience to join their team.
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You will conduct discovery and translate clients’ research and business questions into actionable analyses to demonstrate data feasibility by leveraging the largest healthcare data ecosystem in the US. In collaboration with colleagues, you will identify and educate clients on the data suppliers in the HealthVerity Marketplace (HVM) that capture the necessary data elements to conduct RWD-based studies and produce regulatory-grade real world evidence (RWE.
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Our comprehensive capabilities and teams include preclinical research, clinical development, translational sciences, autologous and allogeneic manufacturing, and in-house commercial and corporate operations.
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The Senior Clinical Director, working closely with the CMO and COO, is responsible for developing and facilitating the quality assurance, risk management, regulatory compliance, and operational performance improvement activities for all clinical services.
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The Wonderful Company has a long-standing commitment to corporate social responsibility, including more than $120 million invested in environmental technologies and sustainability research, $45 million in charitable giving and education initiatives every year, $30 million toward the construction of a new charter school campus in California's Central Valley, and innovative health and wellness programs, including two new, free primary care clinics for employees and their dependents.
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Responsible for meeting clinical productivity targets as determined by Department Chair and/or Directors of Company sites. Direct clinical services to be provided at Company sites.
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Document the psychological assessment, evidence-based, time efficient treatment interventions, and treatment plans in a timely and appropriate manner, to maintain thorough records in compliance with regulatory and insurance requirements.
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Kyowa Kirin is a fast-growing global specialty pharmaceutical company that applies state-of-the-art biotechnologies to discover and deliver novel medicines in four disease areas: bone and mineral; intractable hematologic; hematology oncology; and rare disease.
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Essential Functions Lead Innovation Team in the research and development of project-related microelectronics including strategy, design, analysis, modeling, development, prototyping, testing, circuit design, ASIC design, systems integration, and production.
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Personal statements summarizing teaching experience, clinical and research interests, and contributions to diversity are strongly encouraged. Temple Health is one of Philadelphia's leading academic medical centers, with 20 clinical departments; 8 Basic Science Departments; 13 Research Center (all of which are engaged in patient care education and research) and more than 1,000 physicians and scientists sharing the mission of bringing innovative treatments to patients.
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At least 5 years' and preferably 10 years' experience in leadership of clinical, educational, and/or research programs. As Division Director, the candidate will have direct accountability for clinical palliative care services at Thomas Jefferson University Hospital and Methodist Hospital, including inpatient consultation, and growth of services for ambulatory, telehealth, and community-based non-oncologic palliative care services.
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clinical research pharmaceutical company regulatory compliance juris doctor jobs in Philadelphia, PA
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