- Merck & Co. (Rahway, NJ)
- Job DescriptionThe Global Clinical Supply (GCS) organization is part of our company's Research Laboratories and is accountable for managing the end-to-end integrated ... clinical supply chain across our company's portfolio to enable...and continuous improvement of the end-to-end processes. The Senior Specialist , GCS Process Steward, is accountable for assuring that… more
- Merck & Co. (Lower Gwynedd, PA)
- Job Description-The PDMB Regulated Bioanalytics Department is seeking a Compliane Senior Specialist and Technical Writer team within the Late Development ... IT platforms, and science to accelerate vaccines and enable late-stage clinical trials through the generation of timely, high-quality regulated bioanalytical data.… more
- Merck & Co. (North Wales, PA)
- …Office (PMO); and Administrative Professionals.Position Description/Summary The GPAM Senior Specialist , Value & Implementation Project Manager (VIPM), is a core ... R&D pipeline and realize its full potential. The Senior Specialist is expected to provide project management leadership and...click here if you need an accommodation during the application or hiring process. As an Equal Employment Opportunity… more
- Merck & Co. (Lower Gwynedd, PA)
- …IT platforms, and science to accelerate vaccines and enable late-stage clinical trials through the generation of timely, high-quality regulated bioanalytical data. ... will be utilized to generate pivotal safety and efficacy clinical patient data required for regulatory filings. -As the...click here if you need an accommodation during the application or hiring process. As an Equal Employment Opportunity… more
- Merck & Co. (Lower Gwynedd, PA)
- …IT platforms, and science to accelerate vaccines and enable late-stage clinical trials through the generation of timely, high-quality regulated bioanalytical data. ... in partner organizations or at external scientific meetings, to write technical reports, and to participate on cross-functional teams-Provides scientific input of… more
- Monster (Springfield, IL)
- Job Summary JOB SUMMARY: Under general supervision, use knowledge of clinical workflow and product use in assessing incoming complaints and hazards. Assist in ... post-market reportability determination. Participate in clinical investigations for reported product incidents and submit adverse event reports. Provide clinical … more
- Health eCareers (Memphis, TN)
- Rang Healthcare is seeking a local contract nurse RN Clinical Document Improvement Specialist for a local contract nursing job in Memphis, Tennessee.Job ... back to the CDI team, providers, and other departments as appropriate.The Clinical Documentation Integrity Specialist (CDIS) is a registered nurse (RN)… more
- Monster (Dallas, TX)
- …with project managers, other Epic analysts, application teams, technical infrastructure teams, and clinical /operational stakeholders. o Participate in ... (EHR) system. The EPIC Analyst will work closely with clinical , operational, and technical teams to ensure...clinical or business workflows relevant to the Epic application (s) supported. o Familiarity with healthcare IT standards (eg,… more
- Monster (Boston, MA)
- …and application of quality assurance and compliance. The Sr. Quality Specialist coordinates GMP activities in support of clinical and commercial Drug ... Job Title: QA Sr. Specialist Location: Boston, MA Shifts available:- (1st-Mon to...and approval of manufacturing documents. . Develop and deliver technical training programs . Supports drafting and revising Quality… more
- Merck & Co. (Lower Gwynedd, PA)
- Job DescriptionJob Description-Sample Management Specialist (P3), Regulated Bioanalytics, Integrated Logistics & Sample -Description-The PDMB Regulated Bioanalytics ... Department is seeking a Senior Sample Management Specialist to join our AdVAnce Sample Management group located at our Company's new state-of-the-art AdVAnce GxP… more
