- Defense Logistics Agency (New Cumberland, PA)
- …item data stock record maintenance, denial processing/research. Conducts studies , analyzes finding, and makes recommendations on substantive operating ... your graduate school has determined to represent one academic year of full-time study . Such study may have been performed on a full-time or part-time basis. If… more
- UPMC (Pittsburgh, PA)
- …$6,000 sign-on bonus and will support various Oncology Disease Center program studies working Monday through Friday daylight hours. The Clinical Research Services ... a disease-specific centers model for conducting clinical trials, CRS provides study development and implementation assistance, submissions to the FDA, IRB… more
- Defense Logistics Agency (New Cumberland, PA)
- …to analyze trends of recurring discrepancies. Conducts operational and systemic studies to causes contributing to physical inventory and location inaccuracies and ... your graduate school has determined to represent one academic year of full-time study . Such study may have been performed on a full-time or part-time basis. If… more
- Pfizer (Collegeville, PA)
- …work as a member of the Patient Data Strategies (PDS) team in helping clinical study teams use assigned patient data technologies. The role will be required to take ... a variety of stakeholders and customer groups to ensure study teams are enabled to implement eCOA in clinical... teams are enabled to implement eCOA in clinical studies efficiently, consistently and with the highest quality and… more
- Parexel (Harrisburg, PA)
- …statistical support, including trial design, protocol and CRF development on specific studies + Lead production and quality control of randomization, analysis plans, ... randomization lists and write statistical methodology sections for inclusion in study protocols + Provide statistical input into Data Monitoring Committee (DMC)… more
- UPMC (Pittsburgh, PA)
- …a disease-specific centers model for conducting clinical trials, CRS provides study development and implementation assistance, submissions to the FDA, IRB ... processing, patient recruitment, study coordination, study -specific training, data collection, and...staff, responsible for timely activation and execution of all studies in the disease center, provides managerial oversight of… more
- CSL Behring (King Of Prussia, PA)
- …Development Medical Writing Deliverables, including Investigators Brochure (IB), the Clinical Study Outline, The Clinical Study Protocol (CSP), The Clinical ... but not limited to the development and maintenance of the IB, the Clinical Study Outline, Regulatory Briefing Books, Module 2 submission Documents for IND, MAAs and… more
- University of Pennsylvania (Philadelphia, PA)
- …specifically early phase, complex clinical trials. Responsibilities include: preparing for study visits, including labeling study kits and preparing visit ... packets; maintaining study supplies, including ordering study kits; assisting with the collection, handling, and processing...site files; ensuring that delegation of authority logs and study team training logs are accurate and up to… more
- UPMC (Pittsburgh, PA)
- …billable to third-party payers, ensuring alignment with Medicare coverage rules, and identifying study -related costs that should be covered by the study sponsor. ... and services. + Synchronizes final coverage analysis with appropriate final study documents. + Maintain up-to-date knowledge of healthcare billing regulations, payer… more
- C&S Wholesale Grocers, Inc. (Bethlehem, PA)
- …minimum 5 years in a Supervisory role. **Qualifications** Associate Degree - General Studies , Bachelor's Degree - General Studies , General Equivalency Diploma - ... General Studies , High School Diploma - General Studies **Qualifications** Associate Degree - General Studies ,...General Studies **Qualifications** Associate Degree - General Studies , Bachelor's Degree - General Studies , General… more
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