Clinical Research Coordinator Associate FSM/CC

Job Summary

Captures non-therapeutic clinical research protocols under the guidance of the Principal Investigator and senior staff, ensuring compliance with regulatory laws and institutional guidelines.

Specific Responsibilities

• Coordinates schedules and monitors research activities and subject preparation for minimal risk studies.
• Supports CRC senior staff in the recruitment, screening, eligibility determination process, enrollment of trial participants, and collection of participant information.
• Performs supportive administrative and regulatory duties related to the study, as assigned.
• Recognizes adverse events, protocol deviations, and other unanticipated problems and reports as appropriate.
• Collects, abstracts, and enters research data.

Minimum Qualifications

• Bachelor’s degree in relevant area of study required.
• Experience working with patients and families in clinical settings preferred.
• Knowledge of biology or medicine gained through education or prior work experience preferred.
• Demonstrates strong written/verbal communication skills and cultural sensitivity.

Benefits

• Health, dental, vision, disability, and life insurance.
• Paid vacation and holidays.
• Paid medical/sick and parental leave.
• Tuition benefits for the employee and dependents.
• Pre-tax and flex spending accounts for commuting and dependent care.
• Moderate retirement savings options.
• Wellness programs.

Professional Growth & Development

• Variety of tools and resources for professional development.

Work-Life And Wellness

• Comprehensive programs and services for navigating life’s challenges and maintaining healthy lifestyles.
• Flexible work arrangements and childcare/senior care programs.

Pay

Target hiring range for this position will be between $51,346-$70,210 per year. Offered salary will be determined by the applicant’s education, experience, knowledge, skills and abilities, as well as internal equity and alignment with market data.

Schedule

N/A