We interpreted Morrisville, PA as Morrisville, PA. Other options include: Morrisville (Greene County), PA
- Humana (Trenton, NJ)
- …driving health outcomes and cost-effective care for our members. We are seeking a Clinical Investigation Lead to provide strategic direction to drive ... owners across Humana to drive solutions forward. In this role you will lead quantitative and qualitative investigations to identify actionable insights and bring… more
- J&J Family of Companies (Horsham, PA)
- …status of clinical study activities + Review and assessment of new clinical study proposals + Lead company sponsored study development from protocol ... Solid Tumor group and will actively participate and may lead aspects of the development, oversight, and execution of...clinical pharmacology, etc.) + Monitor, review and analyze clinical trial data + Assist with investigation … more
- SERV Behavioral Health System (Lawrenceville, NJ)
- …and reporting components of the organization. + Conduct ongoing review of clinical supervisor/ lead counselor case files to ensure compliance with federal, ... Counseling, Substance Abuse Disorder. JOB SUMMARY: Responsible for overseeing the clinical and administrative operations of service delivery for the assigned county… more
- Endo International (Horsham, PA)
- …reviews controlled documents (eg SOPs) required for compliance. Quality Systems & CAPA Investigations + Contributes to and may lead operational teams in the ... Review + Supports the QA batch release functions for cGMP commercial, clinical , and development manufacturing and distribution activities from the local, contract… more
- Integra LifeSciences (Princeton, NJ)
- …products/processes from R&D to full-scale manufacturing, following Design Control Procedures. + Lead and manage efforts to create novel processes, leading to full ... new and/or improved processes. + Apply experience with manufacturing process equipment to lead the selection and/or design of equipment from prototype and full scale… more
- Serco (Fort Dix, NJ)
- …staff meetings, training workshops and community meetings. + Coordinate with regional site lead and team members to ensure all program data required for reporting ... **A US citizenship.** + **Must successfully undergo a background investigation (National Agency Check) and able to obtain a...in Social Work, Psychology, or related behavioral health or clinical degree and 2 years of professional experience. +… more
- Taiho Oncology (Princeton, NJ)
- …and evolving needs of patients. Advanced technology, a world-class clinical development organization, and state-of-the-art facilities: these and other resources ... assigned to him/her, including review and analysis of safety data from clinical trials and from post-marketing sources, providing medical expertise to assigned… more
- Takeda Pharmaceuticals (Trenton, NJ)
- …identifying, evaluating, and screening qualified research sites for company sponsored clinical investigation + Actively participates in executing USMAO strategy ... molecular pathways, mechanism of action Takeda Oncology products including clinical outcomes and research opportunities. + Formulate and keep...at medical conferences and may "co- lead " a medical conference to inform for being a… more
- Kelly Services (Plainsboro, NJ)
- …regulatory guidelines for Medical Device Manufacture. As required, conduct Non-Conformance Investigations , assist or lead in the prompt implementation of ... personnel from Engineering, Manufacturing, Product Development, Marketing, QA, and Clinical & Regulatory Affairs. + Effectively implement problem solving skills… more
- BeiGene (Hopewell, NJ)
- …compliance with FDA/EU regulation, covering cGMP for commercial medicinal products and clinical material for human use. + Significant participation in regulatory and ... carry out the review and release of materials and product for commercial and clinical products in accordance with cGMPs. + Ensuring appropriate investigation of… more
- BeiGene (Hopewell, NJ)
- …compliance with FDA/EU regulation, covering cGMP for commercial medicinal products and clinical material for human use. + Significant participation in regulatory and ... review and approval of batch documentation and product release for commercial & clinical products in accordance with GMPs. + Ensuring appropriate investigation … more
- Catalent Pharma Solutions (Somerset, NJ)
- …Supports problem resolution and communication to all affected internal departments. + Lead investigations related to material discrepancies and Trackwise events ... business unit. On site we have our state-of-the-art laboratory, clinical , and commercial manufacturing plant for oral dose forms...chain + Maintain trackers of Order status, PO status, lead time, and receipt for all goods + Source… more
- Merck (West Point, PA)
- …authoring of regulatory submissions and support of significant manufacturing investigations . The group is responsible for establishing the science, engineering ... scientist/engineer, to advance and commercialize Innovative Large Molecules to clinical and commercial manufacturing sites. This person would be accountable… more
- Merck (West Point, PA)
- …authoring of regulatory submissions and support of significant manufacturing investigations . The group is responsible for establishing the science, engineering ... scientist/engineer, to advance and commercialize Innovative Large Molecules to clinical and commercial manufacturing sites. This person would be accountable… more
- Merck (West Point, PA)
- …specifically in the areas of discovery sciences, preclinical development, clinical development, regulatory affairs, and lab supplies and equipment, within ... + Supplier Performance Management - supplier performance monitoring, root cause investigation , issue management, risk assessment and mitigation + Strategic Analysis… more