Clinical Research Coordinator-Neonatal

Children’s Hospitals and Clinics of Minnesota•St. Paul, MN

17h•Onsite

About The Position

Children's Minnesota Neonatology is the largest in Minnesota and one of the largest in the country welcoming over 2,300 babies every year. Research for this department operates on Minneapolis and St Paul campuses, providing a range of level II to level IV clinical care with 180 beds and approximately 2,300 admissions per year. Neonatal research includes a mix of business and industry sponsored studies as well as investigator-initiated internally and externally funded studies, both observational and interventional projects. The Clinical Research Coordinator (CRC) serves as the project manager for assigned projects and works directly with the Research Program manager and Clinical Research Associates I & II to coordinate and implement studies.

Requirements

Baccalaureate in a health-related field and at least four years of clinical research-related experience; or registered nurse with a current license to practice, and at least two years of clinical research experience; or two years of clinical research-related experience and a master's degree in a related field.
The CRC must be a detail-oriented person with strong writing, communication, and computer skills; (s)he must have the ability to manage multiple projects.

Nice To Haves

At least one year of experience working with children is preferred.
SoCRA or ACRP certification preferred.

Responsibilities

Organize and manage all aspects of assigned research activities and ensure compliance with study protocols and overall clinical research objectives
Contribute methodological and technical expertise in the design, implementation, analysis and reporting of research
Prepare regulatory submissions to the Institutional Review Board, and maintain compliance with all federal and local agencies in accordance with Good Clinical Practice guidelines
Provide support to the preparation and management of grants
Perform budget preparation and management, as needed
Facilitate and manage study-related communications (including, but not limited to communication with investigators, collaborators, regulatory bodies, and site monitors)
Proficiency at Interacting with patients and families for securing informed consent, scheduling research visits, and collection of data
Oversight of data collection and entry processes
Manage personal career development and administrative tasks