- Johns Hopkins University (Baltimore, MD)
- …regarding efficient care delivery models, staffing analyses, performance improvement, clinical and administrative systems enhancements, regulatory requirements, ... department and divisional leaders, as appropriate, on ambulatory practice initiatives, clinical program development, or regulatory compliance issues. + Direct… more
- Amgen (Washington, DC)
- …in life sciences or medically related field, including 4 years of biopharmaceutical clinical trial experience ( clinical research experience obtained working ... lasting impact on the lives of patients as we research , manufacture, and deliver innovative medicines to help people...of patients while transforming your career. R&D Supplier Governance Monitor **What you will do** Let's do this. Let's… more
- Dana-Farber Cancer Institute (Boston, MA)
- …systems such as EHR (Electronic Health Record, Inventory Management Systems and other clinical research systems to complete and document duties. Troubleshoots as ... study supply. + May be assigned to areas of Research Pharmacy such as receiving, processing, monitor ...+ Strong attention to detail. + Ability to utilize clinical research platforms/systems. + Ability to support… more
- Wayne State University (Detroit, MI)
- …Essential functions (job duties): Perform laboratory based scientific techniques or clinical /population science (human subjects) research . Design and perform ... studies by developing surveys and interviewing candidates. Participate in implementing research objectives, ensuring compliance with all legal, regulatory and… more
- UPMC (Pittsburgh, PA)
- …monitoring and improvement, and work with management to implement these improvements. + Research clinical trial related questions and provide follow up advice. + ... the development of computer-based module training. + Review and monitor adherence to research compliance policies and...work independently and as part of a team. + Clinical Research Professional Certification or related certification… more
- Lilly (Indianapolis, IN)
- …and experience in synthetic process or formulated product development to enable clinical trials, regulatory submissions, and new product commercialization. This ... drug products, and/or drug product intermediates (eg, spray-dried dispersions), enable clinical programs, and author regulatory submissions. + Support internal… more
- Astellas Pharma (Northbrook, IL)
- …in gastroesophageal or thoracic oncology or immuno-oncology in solid tumors + Prior clinical research experience in an academic setting + Experience in all ... clinical study team to advance one or more clinical trials. Serves as Medical Monitor w/...DSURs and other critical documents. + Able to assimilate Research , Clinical Pharmacology, Biomarker, medical safety, Toxicology… more
- Penn Medicine (Philadelphia, PA)
- …in this regard. Provides ongoing continuing education and skill validation of clinical staff. Quality, Patient Safety, and Regulatory Affairs: Partnership with ... alignment with Health System Requirements. In conjunction with the Vice-Chair of Regulatory Affairs, develop programs that enhance the clinical decision-making,… more
- Johns Hopkins University (Rapid City, SD)
- …based on specific division or department needs._ Classified Title: Sr. Clinical Research Coordinator II Role/Level/Range: ACRP/04/MC Starting Salary Range: ... and tools for data collection, eg participant interviews, administer questionnaires, background research , laboratory processing, etc. + Monitor and ensure team… more
- Sanford Health (Sioux Falls, SD)
- …weekly lab meetings. Participates in the development of protocols, revisions, amendments and monitor plan and scope. Maintains records of research . Compile and ... analyze data. Make figures and graphs to represent data. Presents results to research group. Responsible for regulatory record keeping and training. Must… more