Clinical Research Coordinator- Diabetes/Endocrine

Children’s Minnesota•St. Paul, MN

21h•Onsite

About The Position

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. The Children's Minnesota Diabetes & Endocrine Research Program conducts industry-sponsored and investigator-initiated clinical trials focused on improving treatment options for children with endocrine and metabolic disorders. Our active research portfolio includes studies in achondroplasia, growth hormone deficiency, obesity, hypothalamic obesity, Prader-Willi syndrome, and Turner syndrome. Through collaborations with leading pharmaceutical companies, academic institutions, and healthcare partners, we provide patients access to innovative therapies while advancing the future of pediatric endocrine care. Our dedicated research team is committed to high-quality clinical research and exceptional support for participating children and families.

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