- 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. (Rahway, NJ)
- Job DescriptionJob Description:The Rahway based Senior Specialist , Global Development Quality Operations, is responsible for independent approval of documentation to ... support GMP clinical supply drug product manufacture, testing, release, and maintenance...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. (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. ... in partner organizations or at external scientific meetings, to write technical reports, and to participate on cross-functional teams-Provides scientific input of… 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
- 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
- Tenethealth (Homewood, AL)
- …maintaining the Department's paper and electronic health record system. The HIM Specialist Sr will have an understanding of privacy and security guidelines related ... sites scanning and uploading medical records into a document management application (ie VitalChart ChartFlow (formerly EvriChart)) for remote coding access, include… 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 (Somerset, KY)
- PRODUCT SUPPORT SPECIALIST , RCM Title | Product Support Specialist Location | Homebased with Travel (Any SOFIE Location) Department | Radiopharmaceutical ... To | Director, Radiopharmaceutical Contract Manufacturing (RCM) OVERVIEW The Product Support Specialist will lead the maintenance of all analytical equipment used in… more
- Monster (Atlanta, GA)
- …Psychological Services and Employee Assistance Program (PS/EAP). Work involves the application of professional knowledge and personal judgment to a variety of ... administrative and technical mental health issues, including delivering psychological assessments and...subject to review and approval of the Behavioral Health Specialist II, Psychologist Sr., or the Director of PSEAP/Chief… 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
- Monster (Tucson, AZ)
- Job Responsibilities Configuration and management of EHR/EMR and other clinical IT applications Analyzes organizational needs and defines functional requirement, ... and patches Works with individual staff members, managers and clinicians, and clinical leadership, to evaluate their EHR training needs and abilities Lead EHR/EMR… more
- BioLife Plasma Services (Pittsburgh, PA)
- …therapy Satisfactorily complete the FDA approved training requirements for BioLife Medical Support Specialist Two years in a clinical or hospital setting More ... clicking the "Apply" button, I understand that my employment application process with Takeda will commence and that the...own at riskAbout the role:The Plasma Center Medical Support Specialist EMT - P is responsible for delivering safe… more
- BioLife Plasma Services (Holland, MI)
- …therapy Satisfactorily complete the FDA approved training requirements for BioLife Medical Support Specialist Two years in a clinical or hospital setting More ... clicking the "Apply" button, I understand that my employment application process with Takeda will commence and that the...Center Manager and will perform as a Medical Support Specialist (Plasma Center Nurse) to support plasma center operations.… more
- BioLife Plasma Services (Houston, TX)
- …therapy Satisfactorily complete the FDA approved training requirements for BioLife Medical Support Specialist Two years in a clinical or hospital setting What ... clicking the "Apply" button, I understand that my employment application process with Takeda will commence and that the...Center Manager and will perform as a Medical Support Specialist (Plasma Center Nurse) to support plasma center operations.… more
- BioLife Plasma Services (Temple, TX)
- By clicking the "Apply" button, I understand that my employment application process with Takeda will commence and that the information I provide in my application ... of Use. I further attest that all information I submit in my employment application is true to the best of my knowledge.Job Description$2500 Sign On Bonus… more
- BioLife Plasma Services (Pearland, TX)
- By clicking the "Apply" button, I understand that my employment application process with Takeda will commence and that the information I provide in my application ... attest that all information I submit in my employment application is true to the best of my knowledge.Job...donor notification of unsuitable test results. The Medical Support Specialist (Plasma Center Nurse) works under the guidance of… more
