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Nurse Practitioner; Clinical Research

Job in Chesterfield, St. Louis city, Missouri, 63005, USA
Listing for: SQRL
Full Time position
Listed on 2026-04-17
Job specializations:
  • Science
    Clinical Research
Salary/Wage Range or Industry Benchmark: 55 - 75 USD Hourly USD 55.00 75.00 HOUR
Job Description & How to Apply Below
Position: Nurse Practitioner (Clinical Research)
Location: Chesterfield

  • $55 - $75/hr based on experience and qualifications
  • Work on Research studies in Neurology, Pulmonology, Endocrinology, and Vaccine!
About Our Client

We are working with an exciting clinical trial site organization with over 25 locations, dedicated to advancing innovative therapies and improving lives by making clinical research more efficient and accessible. They focus on large-volume recruitment and retention of diverse and specialty patient populations, and have an experienced team with extensive physician partnerships to help deliver high-quality data across a wide range of therapeutic areas!

The Role

The Sub-Investigator (Clinical Research NP) is responsible for oversight and execution of clinical trials that test new medications on behalf of sponsor/pharmaceutical companies. You will work in an oncology clinic to promote Good Clinical Practice and follow research protocols assigned alongside the PI. You will work along a lead Physician (Principal Investigator) and have a team of skilled coordinators, managers, and assistants as well.

  • Evaluate and screen potential subjects based on study eligibility criteria
  • Perform and review medical procedures in accordance with the clinical study protocol
  • Complete all documentation, paper and electronic
  • Provide oversight and ensures proper delegation of duties to appropriate staff
  • Provide and maintain updated study related documentation
  • Evaluate and report safety reports, protocol noncompliance and any other protocol specific reports.
  • Medical management of patients on trial
  • Administering medications including IV
  • Tracking and management of adverse events
  • Monitoring
Qualifications
  • Ability to dedicate a full time schedule on site in Chesterfield, MO
  • Prior experience working in Clinical Research
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