Clinical Research Coordinator

Piper Companies is seeking a Clinical Research Coordinator for a contract to hire opportunity. This position s is 100% onsite in Philadelphia, PA. The Clinical Research Coordinator supports clinical trials within the Emergency Medicine Department by managing day-to-day research operations, ensuring regulatory compliance, and facilitating collaboration among investigators and study participants.



Responsibilities of the Clinical Research Coordinator:

• Coordinate subject enrollment and manage informed consent documentation.
• Oversee study protocols and ensure compliance with FDA, IRB, and state regulations.
• Maintain and update subject databases and research records.
• Submit research activities and documentation in accordance with IRB guidelines.
• Monitor study payments and ensure timely processing and receipt.

Qualifications of the Clinical Research Coordinator:

• Minimum of 2 years of experience in clinical research coordination.
• Strong knowledge of FDA, IRB, and Pennsylvania research regulations.
• Proficiency in managing multiple protocols and working with diverse investigators.
• Excellent organizational and time management skills.
• Ability to work independently and adapt to changing priorities.
• Strong communication and interpersonal skills.
• Willingness to work flexible hours, including nights and weekends.
• Bachelor’s degree in a health-related field or equivalent experience; advanced degree preferred.

Compensation for the Clinical Research Coordinator:

• Hourly Rate: $$33-$36 ***depending on experience***
• Comprehensive Benefits: Medical, Dental, Vision, 401K, PTO, Sick Leave if required by law

Keywords:

Clinical trials, Emergency Medicine, IRB compliance, FDA regulations, subject enrollment, informed consent, research coordination, protocol management, data integrity, flexible schedule

This job opens for applications on 9/3/25. Applications for this job will be accepted for at least 30 days from the posting date

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