Clinical Research Coordinator II — Protocols & Compliance

Washington University in St. Louis; St. Louis (MO); On-site; USD 55,000 - 75,000; Full time

Job summary

Washington University in St. Louis is seeking a Clinical Research Coordinator to assist investigators in coordinating a complex study across multiple sites. You will manage study procedures, protocol compliance, data collection, and communications with the sponsor, participants, and team.

Qualifications include a Bachelor's degree, 2 years of clinical research experience, and BLS certification. Proficiency with SAS and documentation, plus strong organizational skills, are essential.

Qualifications

• Bachelor's degree or equivalent combination of education and experience.
• 2 years of clinical research experience.
• Basic Life Support certification (BLS) required.

Responsibilities

• Coordinate development and implementation of study procedures.
• Ensure protocol compliance and regulatory documentation.
• Manage data collection, entry, and quality checks.
• Communicate with investigators, sponsors, and participants.
• Prepare manuscripts, amendments, and progress reports as needed.

Skills

Clinical Research

Clinical Study Protocols

Database Management

Research Projects

Spreadsheet Analysis

SAS

Education

Bachelor’s degree or equivalent combination of education and experience

Tools

SAS

Job description

Washington University in St. Louis is seeking a Clinical Research Coordinator to assist investigators in coordinating a complex study across multiple sites. You will manage study procedures, protocol compliance, data collection, and communications with the sponsor, participants, and team.

Qualifications include a Bachelor's degree, 2 years of clinical research experience, and BLS certification. Proficiency with SAS and documentation, plus strong organizational skills, are essential.