- Parexel (Harrisburg, PA)
- **Job Purpose:** The Senior Clinical Research Associate (Sr. CRA) is responsible for the site management, site monitoring and close-out of assigned clinical ... the set-up, running and close-out of sites in a clinical trial . **Key Accountabilities:** **Oversight of Monitoring...Partners with other Study Team members (eg Clinician, Recruitment Specialist , Clinical Data Scientist) + May act… more
- UPMC (Pittsburgh, PA)
- …visit. The specialist maintains and adjusts financial data within the clinical trial management systems (CashFlow/OnCore) and ensures alignment with UPMC's ... Purpose: Under direction of the Senior OnCore Administrator, the OnCore Financial Specialist...and manage sponsor invoicing to ensure timely payment for clinical trial activities + Reconcile payments based… more
- Veterans Affairs, Veterans Health Administration (Coatesville, PA)
- …program office after complete review of the EDRP application. Responsibilities The Senior Social Worker is a professional licensed clinical social worker ... who functions as the Case Management Specialist in the Housing and Urban Development (HUD) Veterans...Reviews all subjective and objective data and makes a clinical assessment, identifying needs and strengths. Provides a concise… more
- Parexel (Harrisburg, PA)
- …limited to (including complex and challenging cases requiring expert judgement)), clinical trial , and literature cases including combination products ... Join our dynamic Patient Safety team as a ** Senior Physician** where you'll leverage your medical expertise...efficiency of drug safety assessments **Skills:** + Experience in clinical medicine (general or specialist qualifications) which… more
- Edwards Lifesciences (Philadelphia, PA)
- …+ Nurse Practitioner or Physician Assistant in structural heart + Experience as a Clinical Specialist , Therapy Development Specialist , Clinical Education ... you'll foster internal and external collaboration to generate and disseminate evidence-based clinical practices to help impact patient lives and advance the quality… more
- University of Pennsylvania (Philadelphia, PA)
- …The Associate Director for Regulatory Affairs will facilitate ongoing improvement of clinical trial compliance and quality assurance through communication of ... with IND/IDE/Expanded Access Applications, drug development process, medical writing, and clinical trial operations required. + Qualified candidates must also… more
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