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Design and execute formulation trials, analytical testing and evaluate stability data to finalize formulation composition for RNA/gene-based therapies. Insight Global is looking for a Formulation Chemist to join the research group for one of our pharmaceutical clients in Bridgewater, NJ. This person will focus on targeted non-viral formulation development for RNA/gene-based therapies.
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This includes planning and oversight of bench- and pilot plant trials. Prepare and oversee pilot plant trials. Support planning (will include ordering/requesting ingredients), execute and manage concept and development trials for medical nutrition and consumer care products as well as VMS products according to project scope/brief.
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This position is a member of the Cell Therapy Development and Operations (CTDO) organization, which supplies autologous and allogeneic cell therapies for first-in-human and pivotal clinical trials.
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Suppliers and the Contingent Worker are responsible for insuring they are fit for all the duties of the job. Mountain RAM) and quality systems software (e.g. Veeva). Must have advanced knowledge and experience with GMP, Quality and compliance.
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Must be fluent in standard Microsoft Office software; experience in asset management software (e.g. Blue Mountain RAM) and quality systems software (e.g. Veeva). Intermediate knowledge of quality systems including CAPA, change control, and document management systems.
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Pharming is seeking to hire a Clinical Trial Assistant (CTA) to bring general administrative support to the Clinical Operations Department and assistance to Project Manager(s), Clinical Project Coordinator(s) and Department Manager/Director(s) on the various tasks associated with conducting clinical trials.
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Commodities managed by this role include Active Pharmaceutical Ingredients, Reference Listed Drugs, Clinical Trials and Services, and R&D Consulting. Additional: International Certifications, such asCertified Purchasing Manager (CPM), Certified Supply Chain Professional (CSCP) or Certified Professional in Supply Management (CPSM.
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Production Worker Location: Waterbury, VTPM Shift Hours: 7:00 pm - 7:30 amShift Pattern: 2/2/3 Pay Rate – $ per hour, with an additional $ shift adjustment and $ shift differential for the 12 PM shift assignments | Weekly Pay PeriodsBenefit OverviewThese are direct hires, full time position with a full benefits package (*Medical, Dental, Vision, 401K, Profit sharing, Tuition/Fitness reimbursement, Paid leaves, Quarterly Bonus payouts, etc.
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Licensed Clinical Social Worker (LCSW)/ Licensed Marriage and Family Therapist (LMFT) / Licensed Professional Counselor (LPC). Licensed Clinical Social Worker (LCSW)/ Licensed Marriage and Family Therapist (LMFT) / Licensed Professional Counselor (LPC.
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They will act as the technical liaison to manufacturing facilities to ensure product quality and food safety during commercialization, with potential travel for product trials and start-ups. Knowledge of non-GMO project, gluten-free and vegan compliance.
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This includes: FDA regulated clinical trials, human subjects research, federally and industry sponsored research. The Research Compliance Auditor is a key contributor to HMH’s Research Compliance Audit and Monitoring Program (RCAMP) which is responsible for post-approval review and auditing of Hackensack Meridian Health Research portfolio for compliance with applicable policies, regulations, and best practices.
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The per diem Social Worker performs social services functions that will assist patients in meeting their bio-psychosocial needs while allowing them to achieve, through therapeutic treatment, their optimal level of emotional health.
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Primary Function: DCA PICKING - PACKING Full Time
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Statistical SAS Programmer Intern Statistical SAS Programmer in Bridgewater, NJ Office Or Waltham, MA Office : Provide statistical programming, data analysis, and data mapping to support clinical trials and FDA submission for new drug development.
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Establishes the conditions essential for determining the safety of all subjects involved in Clinical trials for the vaccine development candidates they oversee. MD is a minimum scientific qualification with 5-10 years pharmaceutical industry experience preferred, with exposure to diverse array of programs in early and late-stage development or 5-10 years or more experience conducting early and late-stage clinical trials in an academic environment.
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trials job Title: worker in Basking Ridge, NJ
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