Senior Clinical Research Coordinator - Trials & Compliance

CU Denver; Aurora (CO); Hybrid; USD 58,705 - 78,665; Full time

Benefits offered by this job

Health insurance

Tuition Benefit

Paid Time Off

Job summary

University of Colorado Anschutz Medical Campus is seeking a Research Services Senior Professional to coordinate and manage clinical research studies involving human participants. You will work with investigators, sponsors, and healthcare teams to ensure studies are conducted safely, efficiently, and in compliance with regulatory requirements.

The role includes overseeing enrollment, data management, protocol procedures, and safety monitoring, contributing to timely study execution and regulatory

Qualifications

• Bachelor's degree in public health, public administration, social/behavioral sciences, physical sciences, nursing, healthcare, finance, accounting, business administration, or a related field; 2 years of professional clinical research experience.
• An advanced degree may substitute for experience if the degree is in a related field.

Responsibilities

• Coordinate and manage enrollment activities, including screening, eligibility, informed consent, education, and scheduling visits.
• Serve as primary contact for assigned trials, ensuring protocol compliance and participant support.
• Oversee specimen collection, processing, documentation, and source documents.

Skills

Clinical research coordination

Participant enrollment

Regulatory compliance

FDA/IRB knowledge

Communication skills

Education

Bachelor's degree in public health or related field

Master's or Doctorate in related field may substitute for experience

Tools

EMR/EHR systems

Data management systems

Job description

University of Colorado Anschutz Medical Campus is seeking a Research Services Senior Professional to coordinate and manage clinical research studies involving human participants. You will work with investigators, sponsors, and healthcare teams to ensure studies are conducted safely, efficiently, and in compliance with regulatory requirements.

The role includes overseeing enrollment, data management, protocol procedures, and safety monitoring, contributing to timely study execution and regulatory