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On-Board Scientific is hiring an Analytical Research and Development Chemist in New Brunswick/Somerset, NJ! Position Details: Position Type: -year contract with additional opportunity contingent upon performance and continued business needJob Location: New Brunswick/Somerset, NJShift: st shiftCompensation: $ per hour (based on experience) The Analytical Research and Development Chemist will work with an assigned project team of chemists in the laboratory to analyze and develop HPLC and GC methods for assay, impurity and dissolution testing of pharmaceutical finished dosage forms.
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Licensed Clinical Social Worker (LCSW)/ Licensed Marriage and Family Therapist (LMFT) / Licensed Professional Counselor (LPC). We are actively looking to hire talented Licensed Therapists in the Princeton Junction, Brick, Eatontown, Piscataway, North Brunswick, Mt Laurel, Lyndhurst and Cherry Hill, NJ area who are passionate about patient care and committed to clinical excellence.
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As a Senior Manager, Global Procurement you will be accountable for supporting the definition and implementation of the global Clinical Core (IRT, eCOA) and Digital Health Technology Category strategy.
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The HORIBA Group of worldwide companies provides an extensive array of instruments and systems for applications ranging from automotive R&D, process and environmental monitoring, in-vitro medical diagnostics, semiconductor manufacturing, and metrology, to a broad range of scientific R&D and QC measurements.
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This individual will support the organization in its build and ramp-up of clinical production and facility approval of a state of the art cell therapy facility. This position will be responsible for maintenance support and mechanical system operations for cGMP Clinical and Commercial Cell Therapy Manufacturing facility.
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He/she/they manages the writing of response to CMC questions from Health Authorities with support from Quality, Global Regulatory Affairs (GRA), technical experts or CMOs. He/she/they performs life cycle management for marketed products by creating and/or evaluating change controls for global regulatory impact and planning corresponding variations/amendments/supplements.
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The Carrier Clinic Part Time Psychologist functions as a clinical psychologist under the supervision of the Chief Medical Officer, in accordance with the Ethical Principles of Psychologists and Code of Conduct of the American Psychological Association, guidelines from the New Jersey Board of Psychological Examiners, and standards set forth by the joint Commission.
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This role partners with the Key Account Manager/Associate Specialty Sales Executive - HCP Marketing Team, and Medical Affairs to execute against strategic imperatives and plans by brand. Medical/clinical selling experience, especially account management, in clinic or office setting with demonstrated success selling to key decision makers including cold calling.
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Report directly to the Administrator, Executive Director or Patient Care Manager Senior and function under the direction, instruction and supervision of the Registered Nurse and/or Clinical Supervisor.
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The Hospice Registered Nurse Liaison is imbedded at Robert Wood Johnson University Hospital and works in a team of Grace Healthcare professionals consisting of other nurse clinical liaisons, a Social Worker, and a Chaplain, all exclusively focused on providing hospice care and end-of-life information to RWJ patients, families, staff and providers.
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Must have experience collaborating with other teams such as Regulatory Affairs, Clinical Development, Quality Assurance, Legal, Clinical Operations, etc. The successful candidate will provide quality expertise to manage and improve processes across Aquestive's development program, ensuring compliance with Good Clinical Practices (GCP), Good Laboratory Practice (GLP), Preclinical stage and GMP for clinical manufacturing oversight.
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Must have Bioanalytical experience so they can help lab troubleshoot issues when applicable, Outsourcing experience preferred but the major focus/must haves should be at least 5 years (with masters or higher degree) or 10 years (with bachelors degree) bioanalytical experience, regulated experience, experience supporting clinical studies, biomarker ops or analysis.
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Reporting directly to the Protein Fortification Research Lead, the Scientist will work at the interface of chemistry and food science and will be responsible for the research and development in plant-based and alternative protein ingredients.
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Masters Degree in Chemistry or related scientific field and 1+ years industry experience as a Chemist. Bachelors Degree in Chemistry or related scientific field and 2+ years industry experience as a Chemist.
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The CMC Regulatory Technical II Writer works closely with quality, manufacturing, Global Regulatory Affairs (GRA), and technical staff from global locations within industrial network, contract manufacturing organizations (CMOs), and alliance partners to author high quality Module 2 and 3 regulatory submissions for both development and post-approval dossiers.
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clinical research scientific affairs jobs Title: director Company: Regeneron Pharmaceuticals Inc in Bridgewater, NJ
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