Pediatric Clinical Research Coordinator

Shriners Children's; Philadelphia (Philadelphia County); Vor Ort; USD 60.000 - 90.000; Vollzeit

Zusammenfassung

Shriners Children's is seeking a Clinical Research Coordinator to coordinate and support pediatric clinical studies. You will help ensure protocols, regulatory requirements, and ethical guidelines are met while assisting patient recruitment, data collection, and documentation within a hospital setting.

Ideal candidates have substantial clinical research experience, familiarity with IRB processes, and knowledge of Good Clinical Practices.

Qualifikationen

• Requires 5+ years of clinical research administration if no Bachelor's degree.
• 3+ years clinical research experience in site management, study management, IRBs, and federal regulations.

Aufgaben

• Maintains a contemporary knowledge of clinical research regulatory requirements.
• Tracks all aspects of projects including study, investigator and IRB information, recruitment activity, and financial management.
• Works with investigators, research leadership, sponsor and regulatory agencies to conduct and report results of clinical research.
• Coordinates data collection, statistical analysis and reporting of results within a clinical study.
• Safeguards all participants involved in research and ensures approvals by Shriners Children's.
• Facilitates local site research programs and projects through timely communications and teamwork.
• Provides consultation and mentorship to site staff, residents, students, and volunteers on research processes and Good Clinical Practices.

Kenntnisse

IRB coordination

Regulatory knowledge

Data collection

Study coordination

Ausbildung

Bachelor's degree in health sciences

Master's degree in clinical research

CCRP or CCRC certification

Jobbeschreibung

Shriners Children's is seeking a Clinical Research Coordinator to coordinate and support pediatric clinical studies. You will help ensure protocols, regulatory requirements, and ethical guidelines are met while assisting patient recruitment, data collection, and documentation within a hospital setting.

Ideal candidates have substantial clinical research experience, familiarity with IRB processes, and knowledge of Good Clinical Practices.