Thank you for your interest in employment at Clinical Research Institute

10/20/21 – Research Coordinator

We are looking for a new research coordinator to join our team!

Job description

Clinical Research Coordinator

Clinical Research Institute has a great opportunity for a Full-Time Clinical Research Coordinator in our Minneapolis, MN office. Clinical Research Institute specializes in Phase II – Phase IV clinical trials for allergy, asthma, migraines, food allergy, vaccines, COPD and atopic dermatitis for all age groups. The Clinical Research Coordinator will oversee start-up procedures, implementation, recruitment, screening, enrollment, and maintenance of study participants while assuring compliance with state and federal regulatory guidelines.

Responsibilities include, but are not limited to:

  • Serves as primary contact for research protocols as delegated by the Principal Investigator (PI)
  • Assumes responsibility of ensuring adherence and proper execution of all protocol procedures and accurate collection of data
  • Source document preparation
  • Create recruitment plan to identify eligible study participants with dedicated Recruitment Specialists
  • Oversee study-specific regulatory matters with dedicated Regulatory Specialist
  • Conduct study participant visits & perform protocol defined procedures (e.g., vital signs, ECG, allergen skin testing, spirometry, etc.)
  • Monitors adverse events and reports per sponsor and IRB-guidelines
  • Maintain research records of study activity, including case report forms, drug dispensation records or other regulatory forms as per FDA guidelines
  • Manage monitor visits, data queries, sponsor audits
  • Interact with physician investigators, clinical staff and industry sponsors
  • Limited travel for attending investigator meetings

Minimum Qualifications/Experience and Education Requirements:

  • Bachelor’s Degree or higher in health-related or life-science field, or equivalent experience
  • Prior clinical trial experience and the ability to understand and implement study protocols
  • Knowledge and understanding of the Federal regulations and guidelines governing the protection of human subjects, e.g. FDA, OHRP, GCP/ICH and HIPAA regulations.
  • Project and time management skills to include the ability to adapt to project changes and priorities
  • Excellent verbal and written communication skills and attention-to-detail; strong interpersonal skills and ability to present information and respond to questions from Investigators and study participants.
  • Must be self-motivated with the ability to think critically and work both independently and as part of a team
  • Proficiency in computer systems such as email, Microsoft Office and familiarity with Electronic Data Capture (EDC) and Clinical Trial Management Systems (CTMS)
  • Experience with phlebotomy/laboratory processing a plus


What we offer:

  • Office hours are 7:30am – 4:30pm Monday – Friday.
  • Competitive compensation and benefits, including health insurance, life & long term disability insurance, 401K with profit sharing along with generous paid vacation/sick time
  • Comprehensive training and professional support for relevant licensure and CRC certification
  • Supportive, respectful, and rewarding work environment

You may learn more about us at CRIMinnesota.com

Send letter of interest, resume and salary requirements to: kari.olson@criminnesota.com

Job Type: Full-time