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Principal Investigator

2 months ago

Jersey City, United States DM Clinical Research Full time
Job DescriptionJob Description

Principal Investigator (MD/DO)

The Principal Investigator will conduct all clinical trials (studies) according to ICH, GCP, local regulations, study protocols, and company processes.

Responsibilities

  • Ensures the medical well-being and safety of the participants through the safe performance and execution of the studies.
  • Assists in maintaining clinical oversight and quality on the studies registered on and delivers on study targets, thereby contributing to the commercial success of the site.
  • Reviews enrollment progress, pre-screening and screening success rates, screen failure rates, safety, and retention of participants.
  • Interprets protocols and IB and participates in initiatives to strategize for patient recruitment.
  • Carries out clinical evaluation and assessment of participants to ensure eligibility to enroll in studies.
  • Ensures and protects the welfare and safety of participants through ethical conduct.
  • Fulfills and complies with all medical duties as per protocol, SOP/COP and ICH GCP and local regulations.
  • Exercises meticulous attention to detail in documentation and patient care.

Requirements

  • Medical license (MD, DO) - New Jersey
  • 2 years experience as a Clinical Research Investigator (Principal Investigator or Sub-Investigator)
  • Bilingual Spanish a plus

Flexible hours - schedule can be tailored as required.

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