Clinical Trials Data Coordinator (Entry-Senior) - Onsite

University of Colorado; Aurora (CO); On-site; USD 50,000 - 79,000; Full time

Benefits offered by this job

Medical options

Dental options

Retirement 401(a)

Paid Time Off

Vacation 22/year

Sick Days 15/year

Holiday Days 15/year

Tuition Benefit

ECO Pass

Job summary

University of Colorado Anschutz Medical Campus in Aurora, CO seeks an Open Rank Data Coordinator (Entry–Senior) to support clinical trials and related research. You will help oversee daily trial operations, collect and verify participant data, and ensure regulatory compliance under the Hematology division.

Role spans entry to senior levels with responsibilities including participant interviews, consent processes, data coding, and coordination of research activities across clinical teams.

Qualifications

• Bachelor’s degree in any field.
• One year clinical research or related experience.
• Two years clinical research or related experience; degree substitution allowed.

Responsibilities

• Assist with and oversee day-to-day operations of clinical trials and studies.
• Obtain medical history and medication data; review eligibility criteria.
• Perform/confirm informed consent documentation.
• Interview prospective subjects and educate on study details.
• Schedule subject participation and coordinate research support.
• Collect, code, and analyze data accurately and timely.

Skills

GCP knowledge

Communication skills

Interpersonal skills

Customer service

Medical terminology

Protocol interpretation

Education

Bachelor's degree in any field

Tools

EMR/EHR systems

Data management systems

Job description

University of Colorado Anschutz Medical Campus in Aurora, CO seeks an Open Rank Data Coordinator (Entry–Senior) to support clinical trials and related research. You will help oversee daily trial operations, collect and verify participant data, and ensure regulatory compliance under the Hematology division.

Role spans entry to senior levels with responsibilities including participant interviews, consent processes, data coding, and coordination of research activities across clinical teams.