Clinical Research Coordinator III; Hybrid; Orthopedic Surgery

Location

St. Louis, MO 63110

40

This position is intended for a highly productive research coordinator with experience managing a large and diverse research portfolio. The ideal candidate will have experience with industry-sponsored studies, federally funded studies, and investigator-initiated trials. Preferred qualifications include prior experience supporting these types of studies, including study coordination responsibilities, assisting with grant writing, and regulatory compliance activities. This is a fast-paced position that requires strong organizational skills, flexibility, and the ability to manage multiple priorities effectively.

Oversees and coordinates more complex clinical research studies; serves as a resource to provide comprehensive information to clinical research staff by promoting a smooth operation, preparation of regulatory compliance and interaction with other departments; may supervise clinical research staff. Coordinates with multidisciplinary teams to maintain continuity of care and human subject protection with a commitment to research integrity.

Primary

Duties & Responsibilities:

• May perform duties inclusive of those delegated to a Clinical Research Coordinator II.
• Responsible for the development of case report forms, questionnaires, and the application of research techniques.
• Reviews and approves the billing matrix calendars for studies.
• Implements and manages all phases of study/protocol lifecycle; ensures compliance with protocol guidelines, standard operating procedures, institutional policies, and requirements of regulatory agencies; monitors participants’ progress; identifies problems and/or inconsistencies with study conduct/data and assists in developing corrective action plans; serves as liaison with funding or sponsoring agency.
• Provides guidance to members of research team in the implementation and evaluation of clinical research; may train new staff; may serve as lead or as point of reference for other research coordinators for questions, staff scheduling, feedback on performance.
• May assist in ordering supplies needed for the research projects and research group.
• Investigator Initiated Research Project Specific Tasks
  • May act as primary liaison to Principal Investigator (PI) to assist in developing plans for investigator-initiated research projects; may assist in preparation of budgets and grant proposals to sponsoring agencies; may assist in writing initial study protocol and instructional manuals; may assist in preparation of amendments to protocols and/or modification to study design, as appropriate.
  • May review 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.
  • May assist in preparation of study progress reports and data safety monitoring reports for PI and funding agencies.
  • May assist in the interpretation of study data and results; may prepare oral and written reports and presentations and/or assist with preparation of manuscripts for publication.
• This position is intended for ahighly productive research coordinator with experience managing alarge and diverse research portfolio. The ideal candidate will have experience with industry-sponsored studies, federally funded studies, and investigator-initiated trials. Preferred qualifications include prior experience supporting these types of studies, includingstudy coordination responsibilities, assisting with grant writing, and regulatory compliance activities. This is afast-paced position that requires strong organizational skills, flexibility, and the ability to manage multiple priorities effectively.

• Performs other duties incidental to the…