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Occasionally a company will reach out for an in person focus group or clinical trial. Remote Work From Home Jobs / Data Entry Clerk - Typing - Work At Home - Doing Data Entry - 100% Remote – Earn Immediately Hello and thank you for your interest.
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Utilize your extensive master data expertise to demonstrate a profound understanding of SAP MDG Materials, BOM, Recipes, MRP, MPS, Work Centers, Batch Management, Quality Inspection, Costing among others.
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BS degree plus minimum 6 years or Master degree plus minimum 4 years of experience OR PhD plus 1 year of experience in Pharmaceutics, Chemistry, Biomedical Engineering, Chemical Engineering, or related field with a strong background in nanoparticle-based formulation development & analytical characterization.
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The Chargemaster Coordinator keeps the Charge Description Master (CDM) current and accurate with regard to changes requested by clinical departments; makes timely updates to the CDM whenever new regulations are published by the Centers for Medicare and Medicaid Systems (CMS); and communicates and coordinates their implementation with changes to the responsible department managers for the Hackensack Meridian Health (HMH) network.
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The Ernest Mario School of Pharmacy at Rutgers, The State University of New Jersey invites applications for a full-time, non-tenure track faculty position in Ambulatory Care. The faculty member will hold a clinical appointment at Hunterdon Medical Center.
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Senior Manager, Tech Ops (Process Chemistry) will have responsibility for the management of API/Intermediate/RSM manufacturing operations at Insmeds CMOs including tech transfer, process optimization, clinical/commercial manufacturing, process characterization and validation, and manufacturing CMC development strategy.
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Lead, direct, coach, and develop an effective Operations team responsible for daily clinical and commercial production of autologous and allogeneic cell therapy products, while ensuring safe and compliant operations according to cGMP requirements.
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Develop and file, in tandem with the General Counsel and the Compliance Office, mandatory insurance regulatory filings related to ERM, including but not limited to the Enterprise Risk Report and the Own Risk and Solvency Assessment (ORSA) Summary Report.
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Join a fast-growing company that specializes in implants made from carbon fiber for patients suffering from spinal tumors.
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Test new tools for the analysis and reporting of clinical research data, analyze updated macros for Pharmacokinetics and Pharmacodynamics data and provide feedback to developers. Develop macro applications that processes biological and clinical data into in-text reports and searchable listings for medical writers for analysis and presentation.
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RN Branch Director, RN Branch Manager, Hospice Branch Director, Executive Director, RN Executive Director, RN Administrator, Hospice Administrator, Hospice Executive Director, Hospice Branch Director, Director of Operations, DON, Director of Nursing, Director of Clinical Operations, Home health administrator, Home health director.
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As a Clinical Manager, you may advance your career into an Area Team Lead or Director of Operations role. Training and advancement: You will enter our Clinical Leadership Program that creates and supports a culture of continuous learning for our managers.
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The Project Manager (PM) leads the coordination of projects, focused on clinical process development, tech transfer and GMP manufacturing of cell and gene based therapies. The Project Manager (PM) leads the coordination of projects, focused on clinical process development, tech transfer and GMP manufacturing of cell and gene based therapies.
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Will consider strong Clinical Fellowship Year (CFY) candidate for Long Term Substitute (LTS) positions in the Related Services program. Master’s Degree in Speech-Language Pathology Pennsylvania Department of Education Certificate in Speech-Language Impaired PK-12 is required Certificate of Clinical Competence in Speech-Language Pathology (CCC-SLP) is required.
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Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market.
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clinical trials trial master file jobs Title: trial master file in Raritan, NJ
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