- Sumitomo Pharma (Harrisburg, PA)
- …a medical safety subject matter expert (SME) on behalf of PVRM for: Study Protocols, Informed Consent Forms (ICF), Safety Management Plans (SMP), Clinical Study ... safety inquiries. + Represents PVRM on post-marketing product specific and/or clinical study team meetings and governance committees. + Performs aggregate review of… more
- Westat (Philadelphia, PA)
- …Assessment Administrators for the 2026 National Assessment of Educational Progress (NAEP) study . NAEP stands as the nation's most comprehensive, ongoing measure of ... with or without reasonable accommodations: + Lift and carry study materials weighing up to 15 pounds to and...collection projects if they become available. Working on this study can be a fascinating, rewarding experience. If you… more
- United Therapeutics (Harrisburg, PA)
- …Bachelor's Degree in life sciences, quality, regulatory affairs or a related area of study or 10+ years of biologic or pharma regulatory experience with a Master's ... sciences, quality, regulatory affairs or a related area of study or 7+ years of biologic or pharma regulatory...sciences, quality, regulatory affairs or a related area of study + 8+ years of project or people management… more
- Pfizer (Collegeville, PA)
- …in clinical trials and supporting development programs. **ROLE RESPONSIBILITIES** Study -level Clinical Development Leadership + Collaborate with Clinical Scientists ... to provide clinical leadership across 2-3 study teams that is scientifically rigorous and aligns with...the point of contact for clinical issues between the study team, investigators, ethics committees, steering committees, and regulatory… more
- Volvo Group (Macungie, PA)
- …world. Interns will be provided extensive hands-on experience in their field of study . The student will work on important and innovative projects alongside our ... but not limited to, geographic location, academic classification, and degree seeking area of study . In addition to these factors, we believe in the importance of pay… more
- Pfizer (Collegeville, PA)
- …demonstrated leadership capabilities. **ROLE RESPONSIBILITIES** Clinical Development Leadership on Study Teams and Development Subteams + Conduct medical monitoring ... + Serve as the point of contact for clinical issues between the study team, investigators, ethics committees, steering committees, and regulatory authorities. + Lead… more
- UPMC (Coudersport, PA)
- …_- Support_ to grow from CRT to RRT, with tuition assistance, paid study time, and exam reimbursement We're offering a **sign-on bonus** for qualified Respiratory ... advantage of **dedicated support, including tuition assistance, exam reimbursement, and paid study time** as they work to become RRTs. + Respiratory Care… more
- Penn Medicine (Phoenixville, PA)
- …and technologists. **Accountabilities:** + Review the patient's history and verify the medical study order + Follow sleep center protocols related to the sleep ... study + Provide age-appropriate patient education + Select appropriate...out of center sleep testing protocols + Analyze sleep study data and prepare reports for provider interpretation +… more
- University of Pennsylvania (Philadelphia, PA)
- …with minimal supervision , regulatory queries, and participate in the initiation of the new study , as well as, communicate transition of the new study to the ... the development and submission of FDA IND applications, and the development of study specific forms and source document tools, as well as, to provide direct… more
- University of Pennsylvania (Philadelphia, PA)
- …Investigator, the Research Specialist will also be responsible for various day-to-day study operations including maintaining study databases, compliance with all ... regulatory documentation, and assisting with the preparation of materials to disseminate study results as needed. Experienced candidates will have the opportunity to… more