- J&J Family of Companies (Titusville, NJ)
- Expert RA Professional Submissions , Submission Management - 2406217374W **Description** Johnson & Johnson Innovative Medicine is recruiting for Expert ... potential. At Johnson & Johnson, we all belong. The Expert RA Professional Submissions...Creates and manages the Dossier Plan(s)/Submission Packages for HA Submissions in line with clinical trials regulatory … more
- University of Pennsylvania (Philadelphia, PA)
- …needed and/or planned and ensure appropriate information is included and addressed. The Regulatory Affairs Specialist C, sends submissions to the FDA, ... needed and/or planned and ensure appropriate information is included and addressed. The Regulatory Affairs Specialist C, sends submissions to the FDA,… more
- Olympus Corporation of the Americas (Center Valley, PA)
- …Manager at 1-888-Olympus (###). Posting Notes: || United States (US) || Pennsylvania (US-PA) || Center Valley || Quality & Regulatory Affairs (QA/ RA ) ... geographic locations you would consider. * Olympus is looking for Global MDR Submissions Analyst II. Hiring Location: US **Job Description** Global MDR Analyst II is… more
- University of Pennsylvania (Philadelphia, PA)
- …trials that offer cutting-edge oncology treatments. Contingent upon funding. The CRU OCCR Regulatory Affairs Office seeks a full-time Regulatory Affairs ... regulatory start-up approvals and associated site initiation documentation. Reporting to the Regulatory Affairs New Study & Continuing Review Manager, the … more
- Takeda Pharmaceuticals (Trenton, NJ)
- …is highly preferred + Advanced education or credentialing in regulatory affairs and project management preferred Demonstrated expert experience leading high ... and Strategic Planning - GI2 TAU within our Global Regulatory Affairs organization, based remotely. + Partners..., to oversee, plan and deliver GRT goals and regulatory submissions in accordance with regulatory… more