Clinical Research Coordinator I

University of Arkansas for Medical Sciences

Little Rock, Arkansas, US
Commensurate with education + experience; not spec...
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Facilitate daily clinical trial activities
Organize complex projects
Attention to detail
** The University of Arkansas for Medical Sciences is seeking a Clinical Research Coordinator I to manage daily activities related to clinical trials. The role requires strong organizational skills, attention to detail, and effective communication as the coordinator will work closely with various stakeholders to ensure compliance with regulations and quality standards. **

Job Summary

  • Position will be directly responsible for facilitating and coordinating the daily clinical trial activities for multiple clinical trials, working closely with investigators, research sponsors, contract research organization representatives, research staff, and UAMS institutional oversight offices.
  • UAMS offers amazing benefits and perks (available for benefits eligible positions only): Health: Medical, Dental and Vision plans available for qualifying staff and family Holiday, Vacation and Sick Leave Education discount for staff and dependents (undergraduate only) Retirement: Up to 10% matched contribution from UAMS Basic Life Insurance up to $50,000 Career Training and Educational Opportunities Merchant Discounts Concierge prescription delivery on the main campus when using UAMS pharmacy.
  • The University of Arkansas is an equal opportunity institution. The University does not discriminate in its education programs or activities (including in admission and employment) on the basis of any category or status protected by law, including age, race, color, national origin, disability, religion, protected veteran status, military service, genetic information, sex, sexual orientation, or pregnancy.

Matching Summary

Match Score: 75

** The University of Arkansas for Medical Sciences is seeking a Clinical Research Coordinator I to manage daily activities related to clinical trials. The role requires strong organizational skills, attention to detail, and effective communication as the coordinator will work closely with various stakeholders to ensure compliance with regulations and quality standards. **

Salary

Commensurate with education and experience; Not specified; Yes

Skills & Requirements

Must-have

  • Facilitate daily clinical trial activities
  • Organize complex projects
  • Attention to detail
  • Communicate effectively
  • Adherence to quality standards

Nice-to-have

  • Teamwork and diversity champion
  • Collaborative healthcare organization
  • Focus on improving patient care

Key Requirements

  • Bachelor's degree plus 3 years
  • High School, GED or formal education equivalent plus 7 years clinical research experience
  • 1-3 years general research experience
  • CRS certification within 2 years of hire
  • Proof of legal authority to work in the United States

Work Rights

Proof of legal authority to work in the United States

Tailored Resume

Cover Letter