Job Description

Piper Companies is seeking a Clinical Research Nurse for a contract to hire opportunity. This position s is 100% onsite in Philadelphia, PA. The Clinical Research Nurse will be responsible for the coordination and execution of clinical trials, combining expert nursing care with regulatory and research responsibilities to ensure high-quality patient-centered research.

Responsibilities of the Clinical Research Nurse:

• Conduct comprehensive nursing assessments, perform clinical procedures (e.g., blood draws, EKGs), and document patient data accurately.
• Coordinate recruitment, screening, and enrollment of research participants, ensuring eligibility and informed consent.
• Schedule and conduct study visits, collect and enter data, and manage subject registration in OnCore.
• Maintain regulatory compliance by preparing and submitting IRB documentation, managing regulatory binders, and attending sponsor visits.
• Perform Epic research billing reviews and triage patient communications related to clinical status, medications, and study participation.

Qualifications for the Clinical Research Nurse:

• Must be a licensed Registered Nurse (RN).
• Certified Clinical Research Nurse (CRN) with hands-on clinical research experience.
• Strong knowledge of regulatory requirements and compliance in clinical trials.
• Proven experience working on industry-sponsored clinical trials.
• Skilled in patient care, including assessments, procedures, and communication.
• Proficient in using clinical and research systems such as Epic and OnCore.
• Experience with IRB submissions and maintaining regulatory documentation.
• Excellent organizational, communication, and data management skills.

Compensation for the Clinical Research Nurse:

Hourly Rate: $40-$45 depending on experience

Comprehensive Benefits: Medical, Dental, Vision, 401K, PTO, Sick Leave if required by law

Keywords:

Clinical Research Nurse, CRN, Registered Nurse, RN, clinical trials, industry-sponsored trials, patient care, nursing assessments, EKG, blood draws, Epic, OnCore, IRB submissions, regulatory binder, research billing review, subject enrollment, data collection, data entry, sponsor visits, clinical procedures, informed consent, regulatory compliance, clinical documentation, medication review, triage calls, clinical research experience, healthcare, medical record documentation, clinical data interpretation, study coordination, research protocols, Good Clinical Practice (GCP), HIPAA compliance, clinical trial regulations, nursing license, clinical monitoring, protocol adherence, patient recruitment, clinical visit scheduling, research ethics, clinical study visits, clinical trial management systems

This job opens for applications on 7/21/25. Applications for this job will be accepted for at least 30 days from the posting date.

#LI-GM1 #LI-Onsite

Job Tags

Hourly pay, Full time, Contract work,

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