Clinical Research Nurse Coordinator - Cell Therapy Safety

Children's Hospital of Philadelphia•Philadelphia, PA

1d•$92,100 - $117,400

About The Position

Children’s Hospital of Philadelphia is seeking a Clinical Research Nurse Coordinator for its Cell Therapy Safety team. The position is Monday through Friday, with the shift based on clinical and operational needs. The coordinator independently manages assigned clinical research activities, applying in-depth clinical research knowledge to coordinate complex studies. The role may include supervisory responsibilities and leadership in the development, implementation, and evaluation of clinical research.

Requirements

Technical Diploma in Nursing.
At least five years of nursing experience.
At least one year of research experience.
Intermediate proficiency with research databases.
Pennsylvania or New Jersey Registered Nurse license within 12 months, or a Pennsylvania or New Jersey Nursing Temporary Practice Permit upon hire.
CPR certification upon hire from an organization requiring hands-on instructor-led psychomotor skills verification, such as the American Heart Association or Red Cross.
Employees working in patient care buildings or with patient-facing responsibilities must receive an annual influenza vaccine.

Nice To Haves

Bachelor’s Degree in Nursing.
At least five years of research experience.
Clinical trial and safety reporting experience.

Responsibilities

Perform all Clinical Research Nurse Coordinator core and additional responsibilities detailed for CRNC I and II.
Apply in-depth knowledge of clinical research and coordinate the conduct of complex studies.
Manage study finances, including sponsor invoicing and resolving study subject billing issues.
Develop advertisement materials, informed consent documents, and Case Report Forms.
Act as a liaison among research subjects, investigators, the IRB, sponsors, and healthcare professionals.
Document investigational product (drug/device) accountability.
Perform self-monitoring and self-auditing responsibilities.
Maintain ClinicalTrials.gov and other relevant systems.
Mentor others in their professional development.
Supervise and train new staff.
Understand good clinical practice (GCP) and regulatory compliance.
Comply with institutional, federal, state, and sponsor policies, standard operating procedures (SOPs), and guidelines.
Take a leadership role in developing, implementing, and evaluating the conduct of clinical research.
Participate in clinical research committees and activities within the assigned division or institution.
Carry out nursing responsibilities and competencies, including physical assessments, taking vital signs, administering investigational drugs, and accessing lines for laboratory tests and pharmacokinetic sampling.