Pediatric Clinical Research Coordinator II

Shriners Children's; Portland (OR); On-site; USD 70,000 - 100,000; Full time

Job summary

Shriners Children's Portland is seeking a Clinical Research Coordinator II to oversee pediatric clinical studies, ensuring regulatory compliance, participant safety, and data integrity on site. The role requires close collaboration with investigators, leadership, and sponsors to ensure high-quality study conduct.

You will manage study information, consent processes, and data collection while adhering to Good Clinical Practices and hospital policies.

Qualifications

• Experience in administration of clinical research with IRBs and federal regulations.
• Experience coordinating site management, study management, and regulatory compliance.
• Knowledge of Good Clinical Practices and regulatory guidelines.

Responsibilities

• Maintains contemporary knowledge of clinical research regulatory requirements.
• Tracks all aspects of projects including study, investigator and IRB information, patient recruitment, and financial management.
• Collaborates with investigators, research leadership, sponsors and regulatory agencies to conduct and report results.
• Coordinates collection, statistical analysis and dissemination of data results in a clinical study.
• Evaluates protocols for feasibility including data collection, entry, storage and reporting.
• Safeguards all participants involved in a SHC-approved study.
• Facilitates local site research programs through timely communications and teamwork.
• Provides mentorship to site staff, residents, students and volunteers on research processes and regulations.
• Interacts with other departments to facilitate research coordination.

Skills

Clinical research

Regulatory compliance

IRB experience

Study coordination

Education

Bachelor's degree in Clinical Research, science or healthcare

Job description

Shriners Children's Portland is seeking a Clinical Research Coordinator II to oversee pediatric clinical studies, ensuring regulatory compliance, participant safety, and data integrity on site. The role requires close collaboration with investigators, leadership, and sponsors to ensure high-quality study conduct.

You will manage study information, consent processes, and data collection while adhering to Good Clinical Practices and hospital policies.