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

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

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

A Clinical Research Coordinator will join our rapidly growing rare lung disease clinical and research center. We perform clinical translational research in patients with rare lung diseases including alpha 1 antitrypsin deficiency and lymphangioleiomyomatosis. The overarching goal of our clinical care and research is to develop strategies to individualize patient clinical

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

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

Medical Laboratory Scientist II Clifton, NJ Sunday to Thursday 9 00AM 5 30PM Perform test procedures of moderate/high complexity requiring the exercise of independent judgement and responsibility in those specialties in which they are qualified by education, training and experience. Must demonstrate proficiency in all areas of testing and be proficient troubleshooting all

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

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

The Senior Embryologist is responsible for executing all the daily functions of the Embryology Laboratory. They are fully competent in all technical aspects of assisted reproductive technology as well as capable of managing the workflow of the lab. The senior embryologist is responsible for monthly reporting to the offsite laboratory director. They work closely with their

At Stony Brook Medicine, a Registered Pharmacy Technician is a valuable member of our team who, under the direct personal supervision of a licensed Pharmacist, assists in compounding, preparing, labeling, and/or dispensing of drugs used to fill valid prescriptions or medication orders or in compounding, preparing, and labeling in anticipation of a valid prescription or me

Follow the laboratory's procedures for specimen handling and processing, test analyses, reporting and maintaining records of patient test result. Maintain records that demonstrate that proficiency testing samples are tested in the same manner as patient specimens. Analyze specimens using approved testing procedures. Review and release test results. Follow CLIA, HIPAA, OSH

Partner cross functionally with internal stakeholders to capture and address sourcing requirements Work closely with Design Engineers and category supply base to reduce no bids and lower costs Identify new sources and negotiate agreements to help meet strategic business objectives Develop and implement sourcing strategies to manage category spend and supply risks Lead sup

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

Establish, manage, and hold direct responsibility over client level disease state portfolio(s). Create and maintain workflows and standards across corresponding clinics and staff. Provide education and industry updates to the team. Maintain responsibility for performance across the portfolio. Have responsibility to serve as an SME to the larger PHS Navigator group. Serve