Clinical Research Coordinator

Vitalief is seeking a Clinical Research Coordinator (CRC) to join their team in Philadelphia. The CRC will support an academic research center and manage concurrent clinical research studies, including NIH-sponsored and investigator-initiated trials. The role involves coordinating patient recruitment, ensuring accurate data collection, and regulatory compliance.

Requirements

• Bachelor’s degree (healthcare or related field preferred).
• Minimum of two to four years of clinical research coordination experience (academic/institutional site experience preferred).
• Strong knowledge of GCP, FDA, and IRB regulations.
• Experience in patient recruitment/retention, IRB submissions, data management, and SAE reporting.
• Proficiency with Electronic Health Records (Epic preferred) and Clinical Trial Management Systems (OnCore preferred).
• Strong Microsoft Office skills (Word, Excel, PowerPoint).
• Excellent written and verbal communication skills.
• Highly organized, detail-oriented, and able to manage multiple priorities.
• Proactive, adaptable, and self-motivated.
• Compassionate, professional demeanor with strong patient interaction skills.
• Phlebotomy certification (or willingness to train)

Benefits

• Competitive benefits including: 20 PTO days + 9 paid holidays
• Company-paid life insurance and short/long-term disability
• 401(k) retirement program
• Comprehensive healthcare plans