Clinical Research Coordinator - Philadelphia, PA

About the role

The Clinical Research Coordinator (CRC) will support the execution of clinical research studies under the direction of a Principal Investigator. Key responsibilities include performing clinical procedures, coordinating study activities, preparing study materials, conducting patient recruitment, managing patient visits, and ensuring data accuracy.

Responsibilities

• Perform clinical procedures such as ECGs, vital signs, and biological sample collection in accordance with study protocols
• Cook up day-to-day clinical trial activities while ensuring compliance with Good Clinical Practices (GCP), protocol, and regulatory requirements
• Prepare study materials, organize equipment, and support overall site readiness
• Conduct patient recruitment activities, including chart review, phone screening, and scheduling study visits
• Perform and manage patient study visits in accordance with protocol requirements
• Educate and orient participants, ensuring a high standard of patient care and safety
• Accurately collect, document, and enter data into Electronic Data Capture (EDC) systems and Case Report Forms (CRFs)
• Resolve data queries in a timely manner and maintain high data quality standards
• Collaborate with investigators, sponsors, and monitors during site visits and audits
• Serve as a patient advocate and maintain a safe, compliant clinical environment

Requirements

• Minimum of 1+ years of clinical research experience in a coordinator or similar role
• Working knowledge of clinical trial processes, Good Clinical Practices (GCP) guidelines, and medical terminology
• Proven ability to conduct patient study visits in accordance with protocol requirements
• Experience in patient recruitment, including chart review and phone screenings
• Proficiency with Electronic Data Capture (EDC) systems, including accurate data entry and query resolution
• Strong attention to detail, organizational skills, and ability to manage multiple priorities
• Effective communication skills and ability to build collaborative working relationships
• Cardiovascular research experience preferred

Qualifications

• Bachelor’s degree preferred, or an equivalent combination of education and relevant experience
• Proven ability to conduct patient study visits in accordance with protocol requirements
• Experience in patient recruitment, including chart review and phone screenings
• Proficiency with Electronic Data Capture (EDC) systems, including accurate data entry and query resolution
• Strong attention to detail, organizational skills, and ability to manage multiple priorities
• Effective communication skills and ability to build collaborative working relationships
• Cardiovascular research experience preferred

Benefits

IQVIA offers a comprehensive benefits package that includes:

• Health insurance
• Retirement savings plan
• Flexible spending accounts
• Employee assistance programs
• Professional development opportunities

Pay

The potential base pay range for this role is $35.00-$42.00 per hour. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time).

Schedule

This is a part-time role, working 24 hours per week.