Clinical Research Coordinator

System One is recruiting for an undisclosed client seeking a Clinical Research Coordinator. The role supports clinical research study coordination and execution, including participant screening and enrollment, study documentation, scheduling, and regulatory compliance.

Responsibilities

• Assist in the coordination and execution of clinical research protocols under the supervision of the PI and senior research staff
• Conduct screening visits to collect medical history & other information from study participants
• Assist with informed consent and enrollment of study participants in accordance with protocol requirements and ethical guidelines
• Coordinate and schedule study visits, procedures, and follow-up activities with study participants and clinical teams
• Collect, record, and maintain accurate clinical research data and source documentation in compliance with regulatory and institutional standards
• Communicate with study participants to provide education, answer questions, and support adherence to study requirements
• Monitor study progress and report adverse events, protocol deviations, and other study-related issues to the research team

Preferred

• an associate's degree or higher in a health-related field preferred
• Experience with participant screening and the informed consent process strongly preferred
• Proficiency with electronic data capture systems, clinical trial management software, and Microsoft Office (Excel, Word, and PowerPoint) preferred
• Current CPR/BLS certification preferred
• Certification as a Clinical Research Coordinator (e.g., CCRC) or a willingness to obtain certification preferred
• Health-related degree
• Participant screening
• Informed consent
• Electronic data capture systems
• Clinical trial management software
• Microsoft Excel
• Microsoft Word
• Microsoft PowerPoint
• CPR/BLS certification
• Clinical Research Coordinator certification

Benefits

• Eligible employees: health and welfare benefits coverage options including medical, dental, vision, spending accounts, life insurance, and voluntary plans
• Eligible employees may participate in a 401(k) plan

Company

• Specialized technical staffing, recruiting, and outsourced workforce solutions.
• Pittsburgh, Pennsylvania, USA
• http://www.systemoneservices.com/
• Founded in 2008
• 5001-10000 employees

Qualifications

• High school diploma or equivalent required
• An associate's degree or higher in a health-related field preferred
• Experience with participant screening and the informed consent process strongly preferred
• Proficiency with electronic data capture systems, clinical trial management software, and Microsoft Office (Excel, Word, and PowerPoint) preferred
• Current CPR/BLS certification preferred
• Certification as a Clinical Research Coordinator (e.g., CCRC) or a willingness to obtain certification preferred

Required skills

• Participant Screening, Informed Consent, Microsoft Excel, Microsoft Word, Microsoft PowerPoint, CPR/BLS Certification, Certified Clinical Research Coordinator (CCRC)

Preferred skills

• Current CPR/BLS certification preferred

Experience

• Entry level