UnitedHealth Group is among the most ambitious Fortune 25 companies you'll ever meet. Through our family of businesses, we're working to make the health care system perform better for more people, in more ways than ever.

Simply put, we think the entire system can be greater than it's ever been. And that drives us to work harder, aim higher, and expect more from one another.

Here, you'll be empowered to make an immediate impact for millions of others. And you'll achieve more than you ever expected. How does that fit with your plans?

UnitedHealth Group is an innovative leader in the health and well-being industry, serving more than 55 million Americans. Through our family of companies, we contribute outstanding clinical insight with consumer-friendly services and advanced technology to help people achieve optimal health. i3 Research i3 Research is a full-service contract research organization (CRO) focused on four CORE areas: central nervous system; oncology; respiratory and infectious disease; and, endocrinology and metabolic disease. Therapeutic specialization drives all aspects of business in this global CRO - from project staffing and talent management to quality initiatives, such as six sigma.   As a UnitedHealth Group company, i3 Research is part of a worldwide health care service organization that uses innovation, integrity and commitment to prepare for the future - and you can prepare for yours with us. It's a rare combination for success that only a career with i3 Research can provide.     The Clinical Research Site Manager (CRSM) interfaces between Clinical Development, Development Operations, and the investigative study sites. The CRSM is expected to independently coordinate and perform activities in the evaluation, initiation, site management, monitoring, and closeout of Clinical Development investigational sites.  The CRSM is responsible for site management and monitoring clinical studies in compliance with good clinical practice (GCP and in accordance with ICH and the FDA Code of Federal Regulations) and acts as the primary contact and liaison between Clinical Development, Development Operations, Study Managers, and investigational study sites to ensure the safety of subjects, the accuracy of data, and the operational success of the site. The CRSM also assists the data management groups and the Study Manager in the processing of all clinical data by ensuring the timely collection of data and query resolution.   Qualifications:   ·                     Bachelor's level degree in life sciences, pharmacy, nursing or RN preferred ·                     2-4  years of clinical monitoring experience ·                     Strong knowledge of Good Clinical Practice/ICH Guidelines and other applicable regulatory requirements ·                     Proven ability to work independently in a fast-paced environment ·                     Strong communication, interpersonal, and organizational skills ·                     Must demonstrate good computer skills ·                     Ability to provide clear direction and guidance to others. ·                     Position requires approximately 60% travel (up to 80% during peak times)     Diversity creates a healthier atmosphere: equal opportunity employer M/F/D/V UnitedHealth Group is a drug-free workplace.  Candidates are required to pass a drug test before beginning employment. Additional Information: Travel Percentage: 75%