- J&J Family of Companies (Spring House, PA)
- …We are searching for the best talent for an **Associate Director, Regulatory Medical Writing** within our Integrated Data Analytics & Reporting (IDAR) business. ... or more of our therapeutic areas within the X-TA Regulatory Medical Writing area. This position is open globally...of TA). + Preparing and finalizing all types of clinical documents, taking a proactive or lead role in… more
- Merck (Upper Gwynedd, PA)
- …+ Work closely with a cross-functional group of experts in commercialization, regulatory affairs, statistics, and manufacturing to manage clinical development ... **Job Description** Our Clinical and Pharmacovigilance teams manage studies to provide...to provide the safety and efficacy data required for regulatory approval of potential new drugs, vaccines and new… more
- University of Pennsylvania (Philadelphia, PA)
- …health and wellness programs and resources, and much more. Posted Job Title Clinical Research Coordinator A/B Job Profile Title Clinical Research Coordinator A ... Job Description Summary As part of the Infectious Disease Clinical Trials Group, this position will coordinate clinical research consisting of projects in HIV,… more
- St. Luke's University Health Network (Allentown, PA)
- …Read, review and understand items related to the Joint Commission and other regulatory requirements. 17. Provides on-call support for clinical equipment. 18. ... of Anatomy and Physiology and Medical Terminology as it relates to clinical equipment. Knowledge of current regulatory requirements. Knowledge of specialty… more
- Merck (North Wales, PA)
- …datasets, tables, listings, figures), the span of which range from individual clinical trials to world-wide regulatory application submissions and post marketing ... art scientific methodologies and tools to enable the discovery, development, regulatory approval, manufacturing, and marketing of medical drugs and vaccines for… more
- University of Pennsylvania (Philadelphia, PA)
- …supervision , the regulatory aspects of the initiation of Phase I-V clinical trials with a focus on required regulatory start-up approvals and associated ... regulatory documentation through the IRB, FDA and all applicable institutional regulatory review committees. In collaboration with clinical research teams and… more
- Merck (North Wales, PA)
- …clinical development, including study design, placement, monitoring, analysis, regulatory reporting, and publication. Specifically, the Director may be ... + Work closely with a cross-functional group of experts in commercialization, regulatory affairs, statistics, and manufacturing to manage clinical development… more
- University of Pennsylvania (Philadelphia, PA)
- …and resources, and much more. Posted Job Title Quality Assurance Analyst ( Regulatory ) CVPF (Center for Cellular Immunotherapy) Job Profile Title Research Coordinator ... Summary The Quality Assurance Analyst will work within the Clinical Cell and Vaccine Production Facility (CVPF) for the...a crucial component of the success of on-going human clinical trials in immunotherapies. Main duties include: + Review… more
- Cardinal Health (Harrisburg, PA)
- …evolution + Collaborate with partners across enterprise, including R&D, Regulatory , Clinical Affairs, Sourcing, Manufacturing, Strategy Functions, Downstream ... Marketing, International Business Partners, etc. + Explore technology and connectivity applications + Support inorganic, or BD&L, pipeline activities + Help identify market opportunities through primary and secondary market research and act by implementing and… more
- Merck (North Wales, PA)
- …+ Work closely with a cross-functional group of experts in commercialization, regulatory affairs, statistics, and manufacturing to manage clinical development ... Principal Scientist) has primary responsibility for planning and directing clinical research activities involving new or marketed cardiovascular and respiratory… more