Senior Clinical Research Coordinator — Study Ops

Washington University in St. Louis; St. Louis (MO); On-site; USD 55,000 - 82,000; Full time

Job summary

Washington University in St. Louis in Saint Louis, MO is seeking a Clinical Research Coordinator to assist investigators as coordinator of a complex clinical study.

You will liaise with the school, sponsoring agency, community and participants to manage all study phases and ensure compliance. The role involves coordinating forms, manuals, data collection, adverse event reporting, and progress assessments within a collaborative research team.

Qualifications

• Bachelor’s degree or combination of education and/or experience may substitute for minimum education.
• Basic Life Support certification must be obtained within one month of hire date.
• Participate in an assigned on call rotation, primarily managing after hours communication and providing support for research operations throughout the week.

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 stop participant inclusion and/or to make and/or recommend adjustment of the protocol of particular participants; resolves protocol management issues and recommends corrective action as appropriate; serves as liaison with funding or sponsoring agency.
• Evaluates and interprets collected clinical data as appropriate; prepares oral or written presentations or reports and analyses setting forth progress trends and provides recommendations or conclusions of the same.
• Performs other duties as assigned.

Skills

Clinical Research

Clinical Study Protocols

Database Management

REDCap

Research Projects

Spreadsheet Analysis

SAS

Education

Bachelor’s degree

Job description

Washington University in St. Louis in Saint Louis, MO is seeking a Clinical Research Coordinator to assist investigators as coordinator of a complex clinical study.

You will liaise with the school, sponsoring agency, community and participants to manage all study phases and ensure compliance. The role involves coordinating forms, manuals, data collection, adverse event reporting, and progress assessments within a collaborative research team.