Perform routine lab tests under thedirection of senior laboratory personnelin those specialties in which they are qualified by education,trainingand experience. Perform and report on assigned analytical testsunder the direction of senior personnelin accordance with applicable Standard Operating Procedures (SOP) ensuring that applicable quality control requirements are met

Roche fosters diversity, equity and inclusion, representing the communities we serve. When dealing with healthcare on a global scale, diversity is an essential ingredient to success. We believe that inclusion is key to understanding people's varied healthcare needs. Together, we embrace individuality and share a passion for exceptional care. Join Roche, where every voice

Educating leadership and clinic staff on the CPS model, to gain their support Initializing and leading ongoing work in clinics and ensuring that the patient/CPS engagement is appropriate and consistent with their preferences. This includes Ensuring that every patient who can benefit from specialty pharmacy services is identified and met in clinic upon arrival Explaining t

The Principal Scientist stability is accountable for the stability program on assigned brand (s) and acts as Stability Product Lead. Participates on transfer team for new products to internal and external sites (as required), reviews registrational stability studies and conducts gap analysis against Global Manufacturing & Supply requirements. Develops stability data where

We are seeking energetic and reliable professionals to join the Zelis team as a Provider Services Specialist. This call center position is primarily responsible for answering inbound calls from providers and healthcare facilities. The Provider Services Specialist ensures providers successfully register for services and navigate the portal to view payment details. Our Prov

Prepares medication orders by compounding or admixing medications under supervision of a registered pharmacist. Checks all orders for completeness of information. Verifies patient information and proper physician authorization. Checks all orders for insurance approval before admixing. Under a professional's supervision, admixes drugs as ordered by physician in an accurate

Laboratory Assistant Job Locations US NY Westbury Job ID 2024 6183 Category Administrative/Clerical Minimum Rate $21.1282 Maximum Rate $21.1282 Work Location Type Physical Overview At New York Blood Center , one of the most comprehensive blood centers in the world, our focus is on cultivating excellence by merging cutting edge innovation with diligent customer service, gr

Currently the Center for Natural Resources has received funding for a few new projects and this position is needed in allocating a skilled resource to one of these projects. We have a project deliverable due in December for which a new employee will be required to assist with oil emulsion tests, analyze and curate the data in CNR laboratory, and also assist with the field

This position is accountable for supporting Pharmacy clinical management. The responsibilities include assisting in formulary management, medication therapy management, utilization management, research and collaboration with disease management and medical management. Responsibilities Supports the pharmacy formulary management program, medication therapy management program

Supports client projects through early translational to late development for clinical pharmacology and quantitative analyses Collaborates with internal and client teams on regulatory, clinical development, clinical, pharmacology, pharmacometric and another drug development issues Assist Project Leaders in writing and compiling reports and other documents summarizing advic

Project Administration Creates and maintains the Trial Master File Management (TMF) Plan. Routinely reviews the TMF to ensure quality, completeness and inspection readiness Coordinates and monitors the activities associated with study deliverables across all applicable internal functional departments and vendors. Assists with activities associated with interim analyses, d

Performs site qualification, site initiation, interim monitoring, site management and close out visits (performed on site or remotely) ensuring regulatory, ICH GCP and/or Good Pharmacoepidemiology Practices (GPP) and protocol compliance. Uses judgment and experience to evaluate overall performance of site and site staff and to provide recommendations regarding site specif

include Assisting in the production of component products Preparing documents and keeping logs associated with receiving, processing and labeling Maintaining equipment and ensuring safe and adequate work environment Maintaining storage areas of carious blood products Shipping and packaging designated products for research and discards Maintaining proper inventory levels of

1. Responsible for the dispensing of inpatient and outpatient medications; verifies prescribed medications according to professional standards, facility procedures, and state and federal legal requirements. 2. Consults with patients regarding medications or supplies prescribed, including dosage, frequency, specialized requirements and possible drug interactions. 3. Works

Trial Preparation Accountable for the execution of monitoring plans & overall quality of monitoring performed by CRAs for assigned US conducted trials (~5 8) across Therapeutic Area(s) phase depending on complexity, size and stage of study. Conduct on site visits to assess CRA performance, including co monitoring/supervisory visits, as requested, including oversight of CR