Job Description

Supports and works closely with the Principal Investigator and research team to administratively coordinate protocol implementation for multiple research studies. CRC conducts day-to day activities of multiple studies with respect to compliance, regulatory, recruitment, study site initiation, monitoring and close out throughout the course of the research trials. The CRC follows protocol, institutional and regulatory requirements to assure accuracy of the study procedures being conducted.

Qualifications

MINIMUM KNOWLEDGE, SKILLS AND ABILITIES:

Education & Training: **** Associate’s degree in related field is required. Bachelor’s degree in epidemiology, sociology, psychology, nursing or field of study related is preferred.

Work Orientation & Experience: At least three (3) years’ experience in clinical research with at least one (1) year of oncology research experience is required. Certified Clinical Research Professional (CCRP) highly preferred. Knowledge of Oncology Clinical Trials, IRB standards and regulatory documentation. Aria experience preferred.

Skills & Abilities: Ability to: (a) organize data management and regulatory aspects of clinical research activity, (b) handle multiple priorities, (c) work independently and take initiative in achieving expected results. Demonstrated skills in: (d) monitoring IRB and FDA clinical research policies and standards, (e) making effective decisions, (f) problem-solving, (g) crisis management, (h) verbal and written patient and staff educational presentations, (i) organizing work, setting priorities, meeting deadlines, (j) attention to detail and follow through, (k) effective negotiation, (l) working with physicians and multiple-specialty team members to obtain clinical data as required by the protocol, (m) ability to work successfully with diverse types of individuals, (n) is computer literate with proficiency in word processing, Excel, and data management software, (o) ability to understand and utilize scientific/medical terminology and research theory in both oral and written communications, and (p) Skill in statistical interpretation and data analysis using statistical software as well as spreadsheet and database software applications.

Additional Information

All your information will be kept confidential according to EEO guidelines.

Compensation:

Pay Range: $30.26- $42.37
Other Compensation (if applicable):
Review the 2025-2026 UMMS Benefits Guide