Clinical Research Support Specialist - Entry Level

University of Colorado System; Aurora (CO); On-site; USD 48,000 - 62,000; Full time

Job summary

University of Colorado Anschutz Medical Campus seeks an entry-level Research Services Professional to support trauma surgery studies. The role involves recruitment, data collection, and coordination across multiple trials, with nights/weekends required and a 40-hour week cap.

Under supervision, you will assist with recruitment, scheduling, data entry, and study support, acting as a facilitator and data manager throughout assigned trials.

Qualifications

• Bachelor's degree in public health, public administration, social/behavioral sciences, physical sciences, nursing, healthcare, biology, or related field from an accredited institution preferred.
• Applicants must meet minimum qualifications at the time of hire.

Responsibilities

• Manage human research subject recruitment and ensure compliance with regulatory policies.
• Assist with study subject activities: chart reviews, recruitment, collecting/processing samples, scheduling visits, and data collection/entry.
• Maintain participant confidentiality with courtesy and respect.
• Assist with data management: collection, entry, and verification for accuracy.
• Build relationships with research subjects, teams, collaborators, and colleagues.
• Adhere to protocol, policy, and regulatory requirements for human subjects research (COMIRB and CITI training).
• Coordinate and manage data from Industry, REDCap, and Oncore; monitor progress of trials.

Skills

Communication skills

Multitasking

Relationship building

Time management

Following procedures

Education

Bachelor's degree (public health/public administration/biomedical fields)

Tools

REDCap

Oncore

Job description

University of Colorado Anschutz Medical Campus seeks an entry-level Research Services Professional to support trauma surgery studies. The role involves recruitment, data collection, and coordination across multiple trials, with nights/weekends required and a 40-hour week cap.

Under supervision, you will assist with recruitment, scheduling, data entry, and study support, acting as a facilitator and data manager throughout assigned trials.