Clinical Research Coordinator: Trials, Compliance & Data

Mercy Home Health; Toledo (OH); On-site; USD 52,000 - 76,000; Full time

Benefits offered by this job

Competitive pay

Medical, dental, vision coverage

Paid time off and leave provisions

Tuition assistance and professional开发

Job summary

Mercy Health is seeking a Research Coordinator to coordinate multiple research projects across Mercy facilities. You will recruit and monitor participants, ensure protocol adherence, and prepare regulatory documents in support of FDA/ICH guidelines.

You will also assist with grant applications, budgeting, and data management while collaborating with investigators, clinicians, and regulatory bodies to advance Mercy Health research initiatives.

Qualifications

• Prior clinical research experience and understanding of the scientific process preferred.
• Ability to write, follow and monitor study protocols, recruit and assist with consenting of study subjects, collect and enter data and follow institutional policies, FDA regulations and ICH/CGP guidelines.
• Excellent written and oral communication skills to write and edit clear, precise scholarly material.
• computer skills necessary to work with a variety of software.

Responsibilities

• Coordinate research projects and monitor protocol compliance across sites.
• Prepare IRB documents and annual/final project reports.
• Assist with grant and study budget applications.
• Recruit and screen subjects and inform relevant staff of project status.
• Act as liaison with investigators, departments, sites, sponsors and regulatory bodies.
• Support sponsor audits, data charts, graphs and publications material.

Skills

Interpersonal skills

Independent work

Written and oral communication

Computer skills

Education

2 Year/ Associates Degree

4 year/ Bachelor Degree

Science or related major

Job description

Mercy Health is seeking a Research Coordinator to coordinate multiple research projects across Mercy facilities. You will recruit and monitor participants, ensure protocol adherence, and prepare regulatory documents in support of FDA/ICH guidelines.

You will also assist with grant applications, budgeting, and data management while collaborating with investigators, clinicians, and regulatory bodies to advance Mercy Health research initiatives.