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The Clinical Chaplain facilitates communication with caregivers outside the healthcare team; serves as a subject matter expert in pastoral care matters and collaborates with community clergy to provide ongoing spiritual support.
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Review CEC/DMC/Clinical trial reports. Provide medical-clinical trial support to sites/investigators that are participating in the clinical research and participate in investigator launch meetings.
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Familiarity with clinical data standards, including CDISC, SDTM, and ADaM , and experience with clinical trial data management systems (e.g., EDC, CTMS). Ensure that the platform enables data visualization and reporting that provides actionable insights into clinical trial performance (e.g., timelines, patient recruitment, data quality.
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In partnership with the research community and other biomedical and clinical informatics specialists, the successful candidate will manage and analyze data being created in molecular and cellular biology, genomics and biomedicine through the use of existing data science and machine learning tools as well as engineer new toolsets that include models, algorithms, and software developed in-house.
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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 years (with masters or higher degree) or years (with bachelors degree) bioanalytical experience, regulated experience, experience supporting clinical studies, biomarker ops or analysis.
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IT System Administration/Vault Owner in Veeva vault (Quality, RIM, Clinical), learning management system (ComplianceWire), validation lifecycle management system (ValGenesis), electronic signature systems (DocuSign.
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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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In-vitro biofilm models and cutting-edge assessment tools will be developed by the Senior Scientist that are predictive of clinical outcomes, provide mechanistic insights or generate new, scientifically robust, claims.
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Collaborate with Protocol Activation office to initiate and activate all new clinical trial protocols assigned utilizing Oncore Study-start up task list. Experience working in a clinical research/trial participant facing role is a big plus (but this is not a requirement - resource will be trained in clinical research.
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Proficient in computer applications (i.e., Microsoft Word & Excel, OnCore™ or other Clinical Trial Management Systems, medical records database systems, etc. Proactively manages, coordinates, and delivers high-quality, compassionate hands-on competent oncology nursing care and coordinates with the assigned clinical team, investigators, and ancillary departments (such as pathology, radiology, clinical laboratory, surgery, infusion services) as per protocol requirements and ensures adherence to the treatment plan and Good Clinical Practice (GCP) guidelines.
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Set-up, organize, and maintain clinical study documentation (e.g. Trial Master File documents, clinical study site documents, email correspondence, training materials, etc.
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Prior experience as a responsible Medical Officer for clinical trial(s) Plan and execute publication and clinical communication strategy in coordination with Scientific Communications.
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The Associate Director will work closely with HEOR team members and others across the company including market access, marketing, medical affairs, and clinical development to support Insmed's business needs.
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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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You will be supported by our Clinical Director and our 24-hour support team. Job Description & Requirements Specialty: Mammography Technologist Discipline: Allied Health Professional Start Date: 10/14/2024 Duration: 13 weeks 40 hours per week Shift: 8 hours, days Employment Type: Local Contract Allied 24/7 is currently looking for Mammography Tech in NEW BRUNSWICK, NJ. This will be a 13-week assignment, 5x8 Days shift starting 10/14/2024 working 40 hours per week.
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clinical job Title: trial master in Somerset, NJ
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