Clinical Research Coordinator I — Study Ops & Compliance

Washington University; St. Louis (MO); On-site; USD 60,000 - 75,000; Full time

Benefits offered by this job

Health insurance

Transit pass

Tuition assistance

403(b) retirement plan

Job summary

Washington University in St. Louis seeks a Clinical Research Coordinator to manage study protocols, ensure regulatory compliance, and coordinate participant activities across visits and assessments.

You will document progress, report adverse events, obtain informed consent, enroll participants, schedule procedures, and prepare progress reports while upholding HIPAA and confidentiality in a collaborative research team.

Qualifications

• Ability to manage protocol phases and regulatory compliance.
• Coordinate participant activities across visits and assessments.
• Maintain accurate documentation and data integrity.

Responsibilities

• Manage all phases of study/protocol and ensure regulatory compliance.
• Contacts/enrolls study participants and determines eligibility based on criteria.
• Obtain informed consent and explain study purpose to participants.
• Administer/scores assessments and schedule EEG testing and related payments.
• Prepare progress reports and analyses of study progress.

Skills

HIPAA compliance

Teamwork

Attention to detail

Communication

Job description

Washington University in St. Louis seeks a Clinical Research Coordinator to manage study protocols, ensure regulatory compliance, and coordinate participant activities across visits and assessments.

You will document progress, report adverse events, obtain informed consent, enroll participants, schedule procedures, and prepare progress reports while upholding HIPAA and confidentiality in a collaborative research team.