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Huron
Research Admin Specialist
atĀ Huron
10 days ago | 68 views | Be the first one to apply

Research Admin Specialist

Full-time
United States, Remote

About the company

At Huron, we’re redefining what a consulting organization can be. We go beyond advice to deliver results that last. We inherit our client’s challenges as if they were our own. We help them transform for the future. We advocate. We make a difference. And we intelligently, passionately, relentlessly do great work…together. Are you the kind of person who stands ready to jump in, roll up your sleeves and transform ideas into action? Then come discover Huron. Whether you have years of experience or come right out of college, we invite you to explore our many opportunities. Find out how you can use your talents and develop your skills to make an impact immediately. Learn about how our culture and values provide you with the kind of environment that invites new ideas and innovation. Come see how we collaborate with each other in a culture of learning, coaching, diversity and inclusion. And hear about our unwavering commitment to make a difference in partnership with our clients, shareholders, communities and colleagues.

Job Summary

Essential Duties:

šŸ“Calendar development for multiple clients including the creation of arms, segments, procedures, and visit assignments in accordance with Huron and industry standards in Clinical Trial Management Systems (ā€œCTMSā€). šŸ“Financial console build including adding protocol related elements, parameters, specifications, subject related items, and milestones for both new and legacy clinical trials in CTMS. šŸ“Coverage Analysis development for multiple clients in accordance with Huron and industry standards both in Excel and in client CTMS. šŸ“Other research administrative back-office deliverable development including by not limited to, budget development and negotiation, sponsor invoicing, account receivable management and reconciliation, and regulatory administrative support.

Required Qualifications:

šŸ“U.S. work authorization is required. šŸ“Bachelor's degree required in a health/science related discipline (biology, public health, healthcare administration, nursing, etc.) or equivalent professional experience. šŸ“A minimum of 3 years of clinical research administration related experience including exposure to coverage analysis, clinical trial budgeting, and/or CTMS calendar or financial console development. šŸ“Ability to interpret and apply clinical guidelines including Centers for Medicare and Medicaid, Federal Drug Administration, National Cancer Network. šŸ“Highly detail oriented with the ability to provide quality assurance or develop back-office research related deliverables with minimal to no errors. šŸ“Intermediate Excel competency šŸ“This is a full time US-REMOTE role. This salaried position may require working additional hours at times, depending on business needs.

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