Clinical Research Coordinator

Position Overview

Join Joulé as a Clinical Research Coordinator based in West Chester/Media, Pennsylvania. This contract role offers a rate between $26 and $30 per hour and requires onsite commitment with a standard 40-hour workweek. There is the potential for transition to permanent employment.

Key Responsibilities

• Support clinical research protocol coordination under the guidance of the Principal Investigator and senior research staff.
• Conduct participant screening to gather medical history and relevant data.
• Facilitate informed consent processes and enroll participants consistent with protocol and ethical standards.
• Manage scheduling of study visits, procedures, and follow-ups liaising with clinical teams and participants.
• Accurately collect, document, and maintain clinical research data in conformity with regulatory and institutional policies.
• Educate and communicate with participants to uphold study adherence and address inquiries.
• Monitor study progress, documenting adverse events, protocol deviations, and other issues.
• Comply strictly with site SOPs and Good Clinical Practice guidelines.
• If qualified, draw, process, and dispatch laboratory specimens including hazardous materials adhering to regulations.
• Organize and maintain study files and records with scanning and filing activities.
• Utilize critical thinking to enhance operational efficiency and resolve challenges.
• Execute additional duties as assigned.

Qualifications and Skills

• Minimum education: high school diploma or equivalent; associate’s degree or higher in health-related fields preferred.
• Basic understanding of clinical research strongly desired.
• Required knowledge of medical terminology and patient care experience.
• Excellent organizational and multitasking abilities with keen attention to detail.
• Effective communication skills capable of engaging diverse populations professionally.
• Team player who thrives in a fast-paced environment.
• Familiarity with GCP, HIPAA, ALCOA standards, FDA regulations, and IATA guidelines preferred.
• Experience with participant screening and consent processes advantageous.
• Proficiency in electronic data capture systems, clinical trial management software, and Microsoft Office suite preferred.
• Medical Assistant certification is a plus.
• CPR/BLS certification desirable.
• Certification as Clinical Research Coordinator (CCRC) or willingness to obtain is preferred.

Additional Information

System One, encompassing Joulé and Mountain Ltd., is a prominent provider of outsourced workforce solutions throughout North America, committed to efficiency and quality. Eligible employees can access health and welfare benefits including medical, dental, vision care, spending accounts, life insurance, voluntary plans, and 401(k) options.

System One is an Equal Opportunity Employer, ensuring fair consideration for all applicants without discrimination based on race, gender, age, disability, or any federally or locally protected characteristic.