Phoenix Children's
Clinical Research Coordinator
Phenix Children’s has a need for a full‑time Clinical Research Coordinator who will lead the coordination of research studies in the NICU and other clinical departments. The position requires a strong focus on regulatory compliance, data integrity, participant recruitment, and study logistics.
Key Responsibilities
Coordinate all phases of clinical studies from enrollment through study closure, ensuring adherence to FDA, OHRP, GCP, and institutional guidelines.
Practice regulatory duties by submitting study documentation to the IRB and institutional committees and maintaining accurate binders and source documentation.
Recruit, interview, and schedule study participants; conduct informed consent and manage participant data via the study database.
Perform data entry of case report forms, maintain source documentation, and track and report adverse events in accordance with sponsor and institutional protocols.
Assist with the feasibility assessment of new studies, create study budgets, and develop workflow procedures for the research team.
Coordinate research monitor visits, respond to data queries, and support the principal investigator and study team with study‑specific education and logistics.
Maintain inventory of supplies and equipment, handle requisitions, and support operational efficiency of study activities.
Required Qualifications
Bachelor’s degree in a related field or equivalent combination of education and experience.
One year of clinical research experience or participation in an approved clinical research training program.
Proven ability to coordinate multiple studies while adhering to regulatory and institutional guidelines.
Strong communication skills for effective interdisciplinary teamwork and participant care.
Certification in Clinical Research (ACRP or SOCRA) preferred; Clinical Research Training Certification and Phlebotomy Certification are additional preferred qualifications.
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Key Responsibilities
Coordinate all phases of clinical studies from enrollment through study closure, ensuring adherence to FDA, OHRP, GCP, and institutional guidelines.
Practice regulatory duties by submitting study documentation to the IRB and institutional committees and maintaining accurate binders and source documentation.
Recruit, interview, and schedule study participants; conduct informed consent and manage participant data via the study database.
Perform data entry of case report forms, maintain source documentation, and track and report adverse events in accordance with sponsor and institutional protocols.
Assist with the feasibility assessment of new studies, create study budgets, and develop workflow procedures for the research team.
Coordinate research monitor visits, respond to data queries, and support the principal investigator and study team with study‑specific education and logistics.
Maintain inventory of supplies and equipment, handle requisitions, and support operational efficiency of study activities.
Required Qualifications
Bachelor’s degree in a related field or equivalent combination of education and experience.
One year of clinical research experience or participation in an approved clinical research training program.
Proven ability to coordinate multiple studies while adhering to regulatory and institutional guidelines.
Strong communication skills for effective interdisciplinary teamwork and participant care.
Certification in Clinical Research (ACRP or SOCRA) preferred; Clinical Research Training Certification and Phlebotomy Certification are additional preferred qualifications.
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