Clinical Research Specialist

2 days ago


New York, New York, United States SQRL Full time

About SQRL

SQRL is a fast-growing site network with over 20 sites across the country, constantly expanding its reach and expertise. Our client is committed to diversity in its trials, covering therapeutic areas such as cardiology, metabolic disorders, renal, CNS, pulmonology, and vaccines. With a focus on excellence in recruitment and retention, SQRL has been recognized for its best-in-class experience for patients and sponsors.

The Role

The Sub-Investigator (Clinical Research NP) is responsible for overseeing and executing clinical trials that test new medications on behalf of sponsor/pharmaceutical companies. Working in a clinic, you will promote Good Clinical Practice and follow research protocols assigned. This includes medical management of patients on trial, administering medications, documentation, tracking and management of adverse events, and overall management of the study. You will work closely with a Principal Investigator and a team of skilled coordinators, managers, and assistants.

  • 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.

Requirements

  • Experience with Clinical Research Studies
  • Nurse Practitioner or Physician Assistant background
  • Ability to dedicate a full-time schedule on site in NYC (Near George Washington Bridge)


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