Epilepsy Clinical Research Coordinator II

Washington University in St. Louis; St. Louis (MO); On-site; USD 54,000 - 82,000; Full time

Benefits offered by this job

Vacation & holidays

Health insurance

Transit pass

Retirement plan

Job summary

Washington University in St. Louis in Saint Louis, MO seeks a Research Study Coordinator to assist investigators on a complex adult epilepsy trial, coordinating multiple studies, liaising with sponsors and participants, and ensuring regulatory compliance.

Bachelor’s degree or combination of education and/or experience, Basic Life Support, and 2 years of clinical research experience are preferred; duties include data collection, protocol management, manuscript preparation, and grant support; SAS

Qualifications

• Bachelor’s degree or combination of education and/or experience may substitute for minimum education.
• Clinical Research experience (2 years) as indicated in Work Experience.
• Proficiency with SAS for statistical analysis as part of duties.

Responsibilities

• Assists in developing plans for research projects and discusses interpretation of results; assists in preparation of manuscripts and grant proposals.
• Coordinates development of forms and questionnaires; assists in writing instructional procedure manuals and literature reviews to aid planning of new studies.
• Implements and manages all phases of study/protocol; ensures compliance with protocol guidelines and regulatory requirements; maintains record-keeping and reports adverse events.
• Prepares oral or written presentations or analyses showing progress trends and conclusions.
• Performs other duties as assigned.

Skills

Clinical Research

Clinical Study Protocols

Database Management

Research Projects

Spreadsheet Analysis

SAS

Education

Bachelor's degree

Job description

Washington University in St. Louis in Saint Louis, MO seeks a Research Study Coordinator to assist investigators on a complex adult epilepsy trial, coordinating multiple studies, liaising with sponsors and participants, and ensuring regulatory compliance.

Bachelor’s degree or combination of education and/or experience, Basic Life Support, and 2 years of clinical research experience are preferred; duties include data collection, protocol management, manuscript preparation, and grant support; SAS