Clinical Research Coordinator

NURA, PLLC; Edina (MN); On-site; USD 55,000 - 75,000; Full time

Job summary

Nura is seeking a Clinical Research Coordinator to perform day-to-day activities supporting clinical research under the direction of the Principal Investigator. The role focuses on participant safety, data quality, and protocol compliance across multiple studies.

Responsibilities include coordinating protocols, screening and enrolling participants, collecting data, and ensuring IRB and regulatory compliance. Strong communication and collaboration with research teams are essential.

Qualifications

• Proven ability to communicate effectively in writing and verbally.
• Proficiency with MS Office and data collection tools.
• Experience in clinical research and patient care preferred.

Responsibilities

• Coordinate research protocols and appointments with study teams and sponsors.
• Screen, recruit, consent, and enroll participants per protocol.
• Collect data and complete case report forms in the EDC; monitor events.

Skills

Communication skills

Attention to detail

Team collaboration

Problem solving

Education

Bachelor's degree in a relevant field

Clinical degree with experience

RN desirable

Tools

Microsoft Office Suite

Job description

Description

Nura is currently hiring a Clinical Research Coordinator! The purpose of this position is to perform the day-to-day activities in support of conducting clinical research at the direction of the Principle Investigator. Provide support to the research team to facilitate the achievement of the program’s goals to ensure: clinical trial participant safety and wellbeing, quality data collection; and compliance to research protocols and all applicable regulations and guidelines.

Essential Functions:

• Coordinate research protocols including arranging necessary research related appointments and procedures, working collaboratively with research team members, other departments, institutions, and sponsors; and maintain contact with study coordinators at other sites or companies, as well as sponsor personnel.
• Screen, recruit, obtain consent from, and enroll research program participants; conduct all research study visits as required by the study protocol.
• Collect study data; Complete case report forms in the EDC; Collect information about medical events and monitor them through the study in coordination with the Principle Investigator.
• Assist research team with sponsor monitoring visits and internal, routine quality control checks.
• Conduct or coordinate training for clinical staff who will be supporting research trials as delegated by the Principle Investigator.
• Possess solid understanding of all applicable federal and state regulations concerning human subject research, as well as drug and/or device trials.
• Identify problems or obstacles in the system/procedures related to implementation of research protocols and communicate them to the study investigators and research team.
• Ensure compliance with all relevant IRB and other regulatory agency requirements.
• Collaborate on the development of research study and program materials including, Informed Consent Forms, educational materials, marketing materials, websites, forms, procedures and reports; Obtain IRB approval for these materials as required.
• Assist in the preparation and submission of IRB documents and reports, as well as filing and maintaining IRB documentation.
• Work with other Research Coordinators and the Principle Investigator to develop, implement, and maintain comprehensive trial master files and research department documentation.
• Maintain study timelines including tracking deadlines for research trials and projects.
• Coordinate with finance and billing to ensure appropriate billing and payment processes.
• Performs other duties as assigned to support the mission, values, and strategies of Nura.

Requirements

Knowledge, Experience & Qualifications:

• Technical degree in the clinical field plus 4 years experience or Bachelor’s Degree in a relevant field, RN highly desirable.
• Minimum 1-2 years of experience in clinical research preferred.
• Excellent communication skills, both written and verbal.
• Proficient with computer applications and software to include Microsoft Office Suite
• Experience within a medical or educational environment preferred.
• Prior work within clinical research or patient care preferred.

Licenses & Certifications:

• Clinical Research Coordinator Certification (CCRC) or Certified Clinical Research Professional (CCRP), preferred.
• A valid driver’s license and proof of insurance required.