Senior Clinical Research Coordinator – Multi-Site Trials

Washington University in St. Louis; United States; On-site; USD 64,000 - 100,000; Full time

Job summary

Washington University in St. Louis is seeking an experienced clinical research professional to oversee and coordinate complex, multi-site studies. You will mentor staff, ensure ethical conduct, and collaborate with multidisciplinary teams to advance research objectives.

Responsibilities include project management, budgeting, recruitment milestones, and regulatory compliance, with opportunities to contribute to grant proposals, study protocols, and manuscripts for publication.

Qualifications

• Education: Bachelor’s degree required; combinations may substitute for minimum education.
• Work Experience: Clinical Research experience (4 years) and Lead position (1 year).
• Certifications/Professional Licenses: Basic Life Support (BLS) issued by AHA or Red Cross; SOCRA/ACRP certification may be required.

Responsibilities

• Oversee and coordinate complex clinical research studies and multi-center trials.
• Mentor and direct research staff; ensure ethics, integrity and collaboration.
• Manage project plans, budgets, recruitment milestones and data safety reporting.
• Assist PI with grant-related tasks, study protocols, and regulatory documentation.
• Prepare progress reports and contribute to publications as needed.

Education

Bachelor’s degree

Job description

Washington University in St. Louis is seeking an experienced clinical research professional to oversee and coordinate complex, multi-site studies. You will mentor staff, ensure ethical conduct, and collaborate with multidisciplinary teams to advance research objectives.

Responsibilities include project management, budgeting, recruitment milestones, and regulatory compliance, with opportunities to contribute to grant proposals, study protocols, and manuscripts for publication.