Clinical Research Coordinator

MercyOne

West Des Moines, IA, US
Not specified; not specified; full benefits pyckag...
Coordinate day-to-day clinical trial activities
Obtain informed consent from study participants
Ensure compliance with good clinical practice
The role supports the execution of clinical trials and research studies for adult patients at the MercyOne Iowa Heart Center West Des Moines

Job Summary

  • The role supports the execution of clinical trials and research studies for adult patients at the MercyOne Iowa Heart Center West Des Moines.
  • Candidates must coordinate study visits, screen participants according to protocol criteria, and maintain inventory of study supplies and drugs.
  • MercyOne offers competitive compensation with a full benefits package and opportunities for growth throughout the system.

Matching Summary

The role supports the execution of clinical trials and research studies for adult patients at the MercyOne Iowa Heart Center West Des Moines.

Salary

Not specified; Not specified; Full benefits package offered

Skills & Requirements

Must-have

  • Coordinate day-to-day clinical trial activities
  • Obtain informed consent from study participants
  • Ensure compliance with Good Clinical Practice
  • Collect and maintain accurate study data
  • Monitor patient safety and report adverse events

Nice-to-have

  • Excellent communication and interpersonal skills
  • Ability to manage multiple tasks and meet deadlines
  • Knowledge of medical terminology
  • Experience in cardiology or research settings

Key Requirements

  • High-school diploma required; Bachelor of Science preferred
  • Valid Iowa Driver's License required
  • Basic Life Support (BLS) certification required within 3 months
  • Mandatory Reporter abuse training required within 3 months
  • Two years critical care or cardiac equivalent experience preferred

Work Rights

Must be eligible to drive per Iowa state law

Tailored Resume

Cover Letter