Clinical Research Coordinator: Impactful Trials

Astera Cancer Care; Lone Tree (CO); On-site; USD 37,000 - 44,000; Full time

Job summary

United Urology Group seeks a Research Coordinator to screen, enroll, and monitor subjects in Phase I–IV trials. You will work with investigators and sponsors to ensure protocol adherence and timely enrollment.

The ideal candidate has a high school diploma and at least 2 years of clinical research experience, with strong attention to detail and effective communication in a fast-paced environment.

Qualifications

• Minimum High School Diploma or GED required.
• Maintained certification of accreditation (CCRC/IATA/CPR/NIH/CITI) required and will be verified prior to employment.
• Strong understanding of FDA clinical trial phases I–IV and GCP standards.

Responsibilities

• Screen, enroll, and follow study subjects for clinical trials.
• Coordinate protocol requirements with PI/SI, Sponsor, and CRO.
• Ensure informed consent accuracy and subject eligibility verification.
• Maintain accurate documentation and regulatory compliance per SOPs and FDA/ICH guidelines.
• Administer study procedures and manage data and drug distribution when applicable.

Skills

Attention to detail

Communication skills

Clinical research knowledge

Safety compliance

Education

High School Diploma or GED

Job description

United Urology Group seeks a Research Coordinator to screen, enroll, and monitor subjects in Phase I–IV trials. You will work with investigators and sponsors to ensure protocol adherence and timely enrollment.

The ideal candidate has a high school diploma and at least 2 years of clinical research experience, with strong attention to detail and effective communication in a fast-paced environment.