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National Marrow Donor Program Clinical Trials Assistant-2000007S in Minneapolis, Minnesota

BE THE MATCH OPERATING PHILOSOPHY:Right now, people's lives depend upon our performance. Our leaders have ownership of their areas, the autonomy to determine the best path, and the responsibility to ethically deliver excellent results. Both team members and leaders exemplify our Be The Match Standards.POSITION SUMMARY:This position will assist the Prospective Research studies teams by performing a variety of coordinating, administrative and data management activities for assigned clinical trials.ACCOUNTABILITIES:Assists with activities related to prospective clinical research projects:Assists study team with trial management logistical support.Creates and maintain study files.Tracks study documents to ensure compliance with regulatory requirements.Tracks and manages study supply shipments to sites and/or participants for assigned studies.Assists with preparation for monitoring visits, including the coordination and management of site visit tasks and internal regulatory file reviews and preparation as appropriate for the assigned study.Assists in managing global communications, and coordinates and sends study documentation to sites (e.g., letters, emails, website posting).Assists study team in the review of consent forms to ensure compliance with protocol and regulatory requirements.Assists team with user acceptance testing of electronic capture systems, both internal and external systems.Assists study teams on study specific data reviews and data cleaning activities.Assists with the preparation, review and maintenance of SOPs, work instructions, training materials, and templates related to project activities.Other duties as assigned.REQUIRED QUALIFICATIONS:Knowledge of:Microsoft Suite of products.Database tracking applications.Customer service skills.Good clinical practices pertaining to data management.Ability to:Perform tasks requiring excellent attention to detail.Enhance the organization's customer service reputation by assisting data management staff, study coordinators, and physicians at sites to resolve questions or concerns.Communicate clearly and effectively to staff and site personnel through oral and written formats.Manage multiple deadlines and priorities while ensuring quality and timeliness.Must exemplify our Be The Match Standards.Education and/or Experience:Bachelor's degree in healthcare/science related field. However, upon evaluation, equivalent related experience and/or education may be substituted for the degree requirement.Minimum one year experience in clinical trials, data abstraction from medical records, or health information management.PREFERRED QUALIFICATIONS: (Additional qualifications that may make a person even more effective in the role, but are not required for consideration)Medical Terminology.Hematopoietic Stem Cell Transplantation process.Equal Opportunity Employer minorities/females/veterans/individuals with disabilities/sexual orientation/gender identity

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