Clinical Research Coordinator II - Oncology

Location: St. Louis, MO 63110

Scheduled Hours: 40

About the role

Assists investigators as coordinator of a complex clinical research study; may be responsible for multiple research studies simultaneously, acting as a liaison with the school, sponsoring agency, community and the study participants; manages and records all phases of study protocol as required by sponsoring agency to ensure compliance.

Responsibilities

• Assists in developing plans for research projects and discusses the interpretation of results
• Collaborates in the preparation of manuscripts for publications and preparation of grant proposals to sponsoring agencies
• Assists in the preparation of amendments to protocols and/or modifications to study design as appropriate
• Coordinates the development of forms, questionnaires and the application of research techniques
• Assists in writing instructional procedure manuals for study progress, data collection and coding
• Reviews journals, abstracts and scientific literature to keep abreast of new developments and to obtain information regarding previous studies to aid in the planning of new studies
• Implements and manages all phases of study/protocol
• Ensures compliance with protocol guidelines and requirements of regulatory agencies
• Establishes record-keeping systems
• Makes assessments and determinations of participants’ progress in the study
• Analyzes, investigates and reports adverse events
• Makes decisions as when to notify physicians of issues, when to