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Endocrinologist (Clinical Trial Physician) - San Juan, PR at ProTouch Staffing San Juan, TX

Fairweather, LLC

San Juan, TX • On-site

$137.76 - $220.42/hr

Other

Posted 3 days ago


Job description

Endocrinologist (Clinical Trial Physician) - San Juan, PR job at ProTouch Staffing. San Juan, TX.

Job Description

Title: Clinical Research Endocrinologist

San Juan, PR | Part-Time (0-8 hours/week)

About the Role

We are seeking a Board-Certified Physician to join as a Clinical Research Physician supporting Phase I-IV clinical trials in San Juan, PR. In this role, you will ensure protocol compliance, patient safety, and collaborate with sponsors, CROs, and research teams to advance multi-therapeutic studies.

Key Responsibilities
  • Serve as Principal Investigator (PI) or Sub-Investigator (Sub-I) for clinical trials.
  • Conduct medical screenings, physical exams, and assessments of study participants.
  • Provide clinical oversight and ensure adherence to study protocols, ICH-GCP, and regulatory standards.
  • Collaborate with coordinators, nurses, and research staff to maintain compliance and accurate documentation.
  • Record patient interactions, manage adverse events (AEs/SAEs), and maintain compliance with EHR/EDC systems.
  • Build and maintain strong relationships with sponsors, CROs, monitors, and IRBs.
  • Participate in site initiation visits (SIVs), monitoring visits, audits, and investigator meetings.
  • Contribute to feasibility reviews, study design, and recruitment strategies.
  • Stay current with clinical research regulations and therapeutic advances.
Qualifications
  • M.D. or D.O. with an active, unrestricted PR medical license.
  • Board Certification in Endocrinology.
  • Valid DEA license and BLS/ACLS certification.
  • Clinical research/clinical trials experience preferred (training available for motivated candidates).
  • Proficiency in EHR systems, medical documentation, and clinical trial platforms (EDC, CTMS).
  • Excellent communication, collaboration, and interpersonal skills.
  • Strong commitment to ethical research and patient-centered care.
Benefits
  • Flexible, part-time schedule (0-8 hours per week).
  • Opportunity to expand expertise in multi-therapeutic clinical trials.
  • Direct involvement in advancing innovative treatments through research.
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