Clinical Research Coordinator

Piper Companies is seeking a Clinical Research Coordinator to join a medical institution located in Philadelphia, PA through an onsite, 3-month, contract-to-hire position. The Clinical Research Coordinator will support clinical investigators with planning, implementing and executing clinical trials within the Emergency Medicine Department.

Responsibilities of the Clinical Research Coordinator include:

• Coordinate study enrollment, manage informed consent documentation, and maintain accurate subject databases and records
• Oversee study protocols and ensure all research activities and submissions comply with IRB, FDA, Pennsylvania state, and related regulations
• Independently manage day-to-day research operations while supporting multiple active protocols and collaborating with multiple investigators
• Facilitate and track study-related payments to ensure timely processing and receipt
• Maintain a flexible work schedule, including availability for evenings and weekends, and perform additional duties as assigned

Qualifications for the Clinical Research Coordinator include:

• Bachelor’s degree in life sciences or a health-related field with 3+ years of directly related CRC experience, or equivalent work history  
• 4–5+ years of clinical trial experience as a Clinical Research Coordinator, including involvement in study start-ups, ongoing studies, and close-outs.
• Comfortability with a full-time “pool group” role, supporting multiple studies across various therapeutic areas (no requirement for deep specialization in a single area)
• Hands-on experience with IRB submissions (local and central), strong eDC data entry skills, and proficiency with MS Office and standard office software
• Excellent written and verbal communication skills, ability to work independently or collaboratively, strong attention to detail, and adherence to project timelines while engaging with diverse populations

 Compensation for the Clinical Research Coordinator includes:

• Pay Rate: $33-$36/hour
• Comprehensive Benefits: Medical, Dental, Vision, 401K, PTO, Sick Leave as required by law, and Holidays

This job opens for applications on 02/07/2026. Applications for this job will be accepted for at least 30 days from the posting date

Keywords: clinical research coordinator, clinical, clinical research, onsite, temporary, life sciences, health sciences, medical, CRC, clinical trial, IRB submissions, eDC, Microsoft, study enrollment, consent documentation, subject databases, records, study protocols, FDA, regulations

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