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Clinical Research Medical Officer

2 months ago

Gurnee, Illinois, United States SQRL Full time

Exciting Career Opportunity

  • Competitive compensation package up to $250,000, plus bonuses and comprehensive benefits
  • Flexible 4-day work week
  • Unique chance to transition into the field of Clinical Research, a rare offering in the industry
  • Work in a more relaxed environment compared to traditional clinical settings, engaging only with patients who choose to participate

About SQRL

SQRL is a rapidly expanding network of clinical sites, currently operating 17 locations and continuously growing. We prioritize diversity in our clinical trials, which encompass various therapeutic areas such as cardiology, metabolic disorders, renal conditions, CNS, pulmonology, and vaccines. Our sites conduct studies across Phases I-IV and have received accolades for excellence in participant recruitment and retention, ensuring a top-tier experience for both patients and sponsors.

Position Overview

The Principal Investigator (Clinical Research Physician) plays a crucial role in overseeing and executing clinical trials that evaluate new medications on behalf of pharmaceutical sponsors. You will operate within a clinical environment to uphold Good Clinical Practice and adhere to assigned research protocols. Responsibilities include medical management of trial participants, administering treatments, maintaining documentation, tracking adverse events, and overall study management. You will collaborate with a dedicated team of coordinators, nurse practitioners, and assistants.

  • Assess and screen potential participants based on eligibility criteria for studies
  • Conduct and review medical procedures in line with clinical study protocols
  • Ensure all documentation is completed accurately, both in paper and electronic formats
  • Provide oversight and delegate responsibilities to appropriate team members
  • Maintain up-to-date study-related documentation
  • Evaluate and report on safety issues, protocol deviations, and other study-specific reports.

Required Qualifications

  • Education: MD or DO degree
  • Board Certification in Internal Medicine or Family Medicine
  • Willingness to commit to a full-time, 4-day per week schedule on-site.