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What you bring: At least 10 years relevant clinical drug safety/pharmacovigilance experience within the pharmaceutical or biotech industry, including 3+ years vendor oversight experience, required.
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7-10+ years of relevant experience in a pharmaceutical company or Medical Communications agency, or at least 15 years of independent Scientific Communications / Publications consultancies for the Pharmaceutical Industry.
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Health Care Professional degree required (e.g., RN/BSN/MSN, NP, PharmD) and 8+ years of pharmaceutical industry experience in drug safety & pharmacovigilance as a Safety Scientist for products in the clinical trial and post-marketing environments or MD with 4+years of clinical experience and 6+years of pharmaceutical industry experience in Safety Science, Clinical Development, or Clinical Research is preferred.
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We are a pioneering pharmaceutical company, reimagining how drugs and services can benefit patients with rare disease to make their lives easier and improve their quality of life. Help shape the culture and future of an emerging pharmaceutical company with a grand vision.
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SUPERVISORY RESPONSIBILITY (if applicable): A Clinical Research Coordinator I does not have any supervisory responsibility. A Clinical Research Coordinator II may assist with the training and orientation of new staff members.
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Demonstrated experience in collaborating with cross-functional teams and teams where you do not have direct authority (AI research, machine learning, biology, medicinal chemistry, pharmacology, pre-clinical sciences, and clinical development.
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Assess: Comparative activity of novel biologics to research-grade control reagents or clinical- stage assets; reliability, repeatability and cost-effectiveness of assay systems. Alloy’s Translational Research team supports our drug discovery partners with in vitro and in vivo testing of therapeutic drug candidates across multiple modalities.
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Work cross-functionally within our Company, including Payer Teams, Field Reimbursement Team, Insight and Analytics, Health Economics and Outcomes Research, Compliance, Legal, and others to understand and build a value proposition for a rare disease medicine(s) that allows for access and reimbursement.
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15 years of clinical research/ biotech/ pharmaceutical experience with at least 7 years experience leading or supporting TMF, clinical document activities, and other Clinical Systems (IRT, CTMS, etc.
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Under the direct supervision of the Metabolism & Nutrition Research Director/Manager and within hospital and departmental guidelines, the Research Diet Technician (RDT) performs a broad range of responsibilities to support research studies on the Translational & Clinical Research Centers (TCRC) on White 12/13 (MGH main campus.
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The Research Scientist will be primarily responsible for overseeing data generation, analysis and interpretation of clinical protocol defined biomarker assays, managing clinical trial biomarker samples, and overseeing external assay development projects at CROs. The successful candidate will be a key member of a multifaceted team that works seamlessly across research and clinical functions to support the clinical biomarker strategies.
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The Research Project Manager (RPM) will have the opportunity to oversee cutting-edge industry and investigator-initiated clinical trials while interfacing with pharmaceutical/biotech experts, research organizations, and physician investigators in a multidisciplinary fashion.
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Chemistry, Clinical Pharmacology, Clinical Research, Clinical Study Reports, Clinical Trials, Data Entry, Drug Discovery, Due Diligence, Electronic Components, Gene Therapy, Lifesciences, Medical Research, Microsoft Office, Modeling And Simulation, Patient Care, Physics, Translational Medicine, Waterfall Project Management.
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Respond to questions from the research and development organization on an as-needed basis, including questions related to conduct of clinical trials in the United States and abroad. 8 – 10 years of relevant experience as a commercial product attorney for a pharmaceutical company and/or life sciences law firm.
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Additionally, the company has research and development sites and commercial offices in North America, Europe, Australia and Latin America. Northeastern University Pharmaceutical Industry Fellowships Program is a two-year experiential program designed to advance lifelong learning and the education and training of Pharm.
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clinical research pharmaceutical company jobs Company: Qps Holdings in Watertown, MA
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