Epilepsy Clinical Research Coordinator II

Washington University

United States

On-site

USD 55,000 - 82,000

Full time

14 days+
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Benefits offered by this job

Vacation & holidays
Metro U-Pass
Retirement plan (403b)
Wellness programs
Caregiver leave
Tuition remission

Job summary

Washington University in St. Louis is seeking a Clinical Research Coordinator to support a complex epilepsy study conducted at Saint Louis, MO.

You will liaise with investigators, sponsors, and participants, and help ensure protocol compliance across all study phases. Responsibilities include developing data collection forms, coordinating procedures, preparing manuscripts and grant proposals, and monitoring adverse events.

Qualifications

  • Bachelor’s degree or combination of education and/or experience.
  • Basic Life Support certification required within one month of hire date.
  • Clinical Research experience: 2 years.
  • Driver's License: A driver's license is not required for this position.
  • Basic Life Support certification (AHA/Red Cross) required.

Responsibilities

  • Assist in developing plans for research projects and interpret results.
  • Collaborate in manuscript preparation and grant proposals for sponsoring agencies.
  • Coordinate the development of forms, questionnaires and data collection procedures.
  • Ensure protocol compliance and manage study records across phases.
  • Monitor adverse events and communicate findings to investigators.

Skills

Clinical Research
Clinical Study Protocols
Database Management
Research Projects
Spreadsheet Analysis
SAS

Education

Bachelor’s degree

Tools

SAS

Job description

Washington University in St. Louis is seeking a Clinical Research Coordinator to support a complex epilepsy study conducted at Saint Louis, MO.

You will liaise with investigators, sponsors, and participants, and help ensure protocol compliance across all study phases. Responsibilities include developing data collection forms, coordinating procedures, preparing manuscripts and grant proposals, and monitoring adverse events.

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