Research Coordinator

Children’s Minnesota•USA, MN, MN and WI Remote, MN

2d•Hybrid

About The Position

Children's Minnesota is seeking a Clinical Research Coordinator (CRC) to serve as the project manager for assigned research projects. This role works directly with the Research Program Manager and Clinical Research Associates I & II to coordinate and implement studies. The CRC will be responsible for organizing and managing all aspects of assigned research activities, ensuring compliance with study protocols and overall clinical research objectives. They will contribute methodological and technical expertise in the design, implementation, analysis, and reporting of research. Key duties include preparing regulatory submissions to the Institutional Review Board, maintaining compliance with federal and local agencies according to Good Clinical Practice guidelines, and providing support for grant preparation and management. The role also involves budget preparation and management, facilitating study-related communications, interacting with patients and families for informed consent and data collection, and overseeing data collection and entry processes. Additionally, the CRC will manage their personal career development and administrative tasks.

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.
Detail-oriented person with strong writing, communication, and computer skills
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