Washington University of St. Louis Medical Oncology in St. Louis, Missouri

Job Type/Schedule

This position is full-time and works approximately 40 hours per week.

Department Name/Job Location

This position is in the Department of Medicine, Division of Oncology. This position is for the Medical School Campus.

Essential Functions

*POSITION SUMMARY: *

Position assists investigators as coordinator of a basic to semi-complex clinical research study; may be responsible for numerous research studies simultaneously, acting as a liaison with the school, sponsoring agency, community and the study participants; responsible for managing and recording all phases of study protocol as required by sponsoring agency to ensure compliance.

PRIMARY DUTIES AND RESPONSIBILITIES:

  1. Implements and manages all phases of study/protocol; ensures compliance with protocol guidelines and requirements of regulatory agencies; identifies problems and/or inconsistencies and monitors participant’s progress to include documentation and reporting of adverse events; resolves IRB/protocol management issues and recommends corrective action as appropriate; serves as liaison with funding or sponsoring agency.
  2. Recruits and enrolls study participants; confers with participants to explain purpose of study and obtain informed consent; explains diagnostic procedures and treatment plans to address participant/family concerns; administers/scores tests and/or evaluates all lab and clinical assessments to ensure they are completed in a timely manner.
  3. Evaluates and interprets collected clinical data in conjunction with PI as appropriate; prepares oral or written presentations or reports and analyses setting forth progress trends and provides recommendations or conclusions of the same.
  4. Collects clinical data under clinical research protocols.
  5. Performs other duties incidental to the work described herein.

Required Qualifications

  • Bachelor’s degree required; prior work experience, preferably in clinical research support, is required.
  • Additional work experience in clinical research can substitute for required education.
  • A combination of work and education equaling 4 years may substitute for this requirement.

Preferred Qualifications

  • SOCRA or ACRP certification required within 24 months of hire or at the time of eligibility.
  • Some experience in a medical office preferred.
  • Working knowledge of computer programs and systems, with communication, organizational and interpersonal skills.

Salary Range

The hiring range for this position is $42,494 - $53,144 annually.

Pre-Employment Screening

Offers made for this position are contingent upon the successful completion of all required pre-employment screens, including a criminal background check, hair sample drug screen, and verification of required professional licenses, registrations, or certifications.

Benefits

  • Retirement Savings Plan

  • 22 vacation days

  • 8 Paid Holidays

  • Sick Time

  • Tuition benefits for employee, spouse and dependent children

  • Free Metro Link/ Bus pass

  • Free Life Insurance

  • Health, Dental, Vision

  • Health Savings Accounts (HSA)

  • Long Term Disability Insurance

  • Flex Spending Plan

  • Other Benefits

Med School HR website (medschoolhr.wustl.edu)

EOE Statement

Washington University is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, age, sex, sexual orientation, gender identity or expression, national origin, genetic information, disability, or protected veteran status.

Job Title: Clinical Research Coordinator I - Medical Oncology - 40693

Job ID: 40693

Location: Medical School

Full/Part Time: Full-Time

Regular/Temporary: Regular