Clinical Research Coordinator I - THRIVE Study (6 Months)

Washington University in St. Louis; St. Louis (MO); On-site; USD 49,000 - 74,000; Full time

Benefits offered by this job

Vacation time

Holiday pay

Health insurance

Metro transit U-Pass

Job summary

Washington University in St. Louis is seeking a Research Coordinator to support the THRIVE study protocol. The role focuses on data collection, wearable device testing, and participant recruitment for a six-month assignment, funded by PCORI.

The position lies in a patient-care setting with regular desk work and clinical duties. Primary duties include coordinating all study phases, ensuring regulatory compliance, enrolling participants, obtaining informed consent, and managing data and reports.

Qualifications

• Bachelor’s degree or combination of education and/or experience may substitute for minimum education.
• Basic Life Support (BLS) certification required.
• No specific prior work experience required for this position.
• Strong communication and organizational skills; familiarity with clinical research processes.

Responsibilities

• Implements and manages all phases of study protocol; ensures regulatory compliance and proper record-keeping; monitors participant progress and reports adverse events.
• Recruits and enrolls participants; confirms eligibility; obtains informed consent; explains procedures and treatment plans to participants and families.
• Ensures timely completion of protocol requirements including assessments, labs, procedures, and treatments; analyzes data and prepares progress reports.
• Collects clinical data under clinical research protocols.
• Performs other duties as assigned.

Skills

Clinical Research

Clinical Study Protocols

Communication

Computer Systems

Interpersonal Communication

Organizing

Research Support

Education

Bachelor’s degree

Job description

Washington University in St. Louis is seeking a Research Coordinator to support the THRIVE study protocol. The role focuses on data collection, wearable device testing, and participant recruitment for a six-month assignment, funded by PCORI.

The position lies in a patient-care setting with regular desk work and clinical duties. Primary duties include coordinating all study phases, ensuring regulatory compliance, enrolling participants, obtaining informed consent, and managing data and reports.