- Johns Hopkins University (Baltimore, MD)
- …& Responsibilities** + Schedule and conduct, monitoring reviews for IRB approved studies + Conduct pre and post enrollment research record reviews for ... **Minimum Qualifications** + Bachelor's Degree. + Three years of related clinical/ medical research experience. + Additional education may substitute for… more
- Dana-Farber Cancer Institute (Boston, MA)
- The **Clinical Research Coordinator (CRC)** will support the Breast Oncology Cohort Studies Program and its clinical and translational research in the areas ... with direction and guidance from the Director and Clinical Research Managers of the overall Cohort Studies ...of related experience preferred. + Experience working in a medical or scientific research setting or comparable… more
- Edwards Lifesciences (Kansas City, KS)
- …+ Bachelor's Degree and a minimum of 5 years of work experience in clinical research monitoring , with a strong focus on quality assurance, quality control, and ... inspiring journey. **How you'll make an impact:** + Field monitoring of studies and data collection for...of cardiovascular physiology and structural heart anatomy + Previous medical device Clinical Research experience in cardiology… more
- Edwards Lifesciences (Jefferson City, MO)
- …acumen and functional skills. + Providing input on strategic direction on field monitoring of studies and data collection for clinical trials with increased ... patients in need. In close partnership with principal investigators, dedicated medical professionals, patient advocacy groups, and regulatory authorities, you will… more
- Arkansas Children's (Little Rock, AR)
- …description for details. **Time Type:** Full time **Department:** CC033007 Research Integrity **Summary:** **Additional Information:** Responsible for monitoring ... Certifications:** **Recommended Certifications:** **Description** 1. Develop, implement, and maintain a monitoring program and tools for human research . 2.… more
- United Therapeutics (Research Triangle Park, NC)
- … support for urgent medical inquiries + Conduct medical monitoring activities for allocated clinical studies + Participate in review and approval ... review and approval of final study reports + Document all medical monitoring activities and communications related to allocated studies + Perform other… more
- Cook Medical (West Lafayette, IN)
- …and global medical device regulations, with experience working on medical device studies highly preferred. Personal Qualifications: * Experience developing ... Overview The Clinical Monitoring Manager is responsible for setting up and...is responsible for setting up and overseeing the Clinical Research Associates (CRAs) in AMER, meeting deliverables, developing procedures… more
- University of Utah (Salt Lake City, UT)
- …land/environmental stewardship, and development of indigenous-led AI tools for environmental monitoring . Qualified candidates may have research interests across ... innovation in AI-enhanced research ; + Conducting and publishing rigorous research topics aligned with environmental monitoring ; + Collaborating in… more
- Johns Hopkins University (Baltimore, MD)
- …at affiliate institutions as needed. + Schedule compliance monitoring visits with research study staff to monitor data integrity studies . + Generate queries ... Specialist_** who will be responsible for conducting compliance monitoring reviews of clinical research trials in...Degree. + Three years of related experience with clinical trials/ medical research . + Additional education may substitute… more
- Rush University Medical Center (Chicago, IL)
- …each case. **Summary:** This positions provides regulatory support for multiple clinical research studies , which may involve multi-centered cooperative group ... required within 1 year of employment. **Responsibilities:** * Supports multiple clinical research studies , which may involve multi-centered cooperative group … more
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