Clinical Research Coordinator: Remote Growth & Mentorship

Filetwigbay; Springfield (IL); On-site; USD 57,000 - 82,000; Full time

Benefits offered by this job

Mentor program

Growth plan

Benefits for life beyond Springfield

Job summary

Dover Corporation is seeking a Clinical Research Coordinator in Springfield, IL. The role emphasizes patient-focused care, mentorship of junior staff, and meticulous clinical operations.

You will work onsite, manage patient status changes, and contribute to reporting while maintaining compliance with manufacturer guidelines. Ideal candidates will have strong organizational skills, a willingness to relocate, and the ability to present to leadership and stakeholders.

Qualifications

• On-site work in Springfield, IL or willingness to relocate.
• Strong organizational skills with ability to juggle multiple workstreams.
• Learner's pace that keeps up with shifting requirements.
• Comfort presenting ideas to mid-level leadership.
• Comfort presenting to stakeholders at all levels.
• Proven leadership experience guiding mid-level initiatives.

Responsibilities

• Mentor junior clinical staff and support onboarding as a mid-level team member.
• Recognize and escalate changes in patient status promptly.
• Maintain a clean, organized, and outcome-focused care setting.
• Operate and maintain clinical equipment per manufacturer guidelines.
• Stock the crash cart and verify expiration dates so nothing fails when seconds count.
• Spot subtle decline early and act before the code is called.
• Set up and break down sterile trays between cases on a tight OR turnover clock.
• Track patient outcomes and contribute to clinical reporting.

Skills

Organizational skills

On-site work in Springfield, IL or rel

Learner pace

Presentation to leadership

Stakeholder communication

Leadership experience

Job description

Dover Corporation is seeking a Clinical Research Coordinator in Springfield, IL. The role emphasizes patient-focused care, mentorship of junior staff, and meticulous clinical operations.

You will work onsite, manage patient status changes, and contribute to reporting while maintaining compliance with manufacturer guidelines. Ideal candidates will have strong organizational skills, a willingness to relocate, and the ability to present to leadership and stakeholders.