Lead Clinical Research Investigator

1 week ago


San Bernardino, California, United States ACRS Holdings Full time
Position Overview

The Catalina Research Institute (CRI), part of ACRS Holdings, is dedicated to advancing clinical trials in complex metabolic and central nervous system conditions. We are currently seeking a Clinical Research Principal Investigator to join our esteemed team.

Role Details

Employment Type: Part-time or Full-time
Location: On-site in California

Qualifications

The ideal candidate must possess a valid California medical license and meet one of the following criteria:

  • MD: Doctor of Medicine

Fluency in both Spanish and English is preferred. Candidates should have a minimum of 3 years of experience in clinical research within the healthcare sector.

Key Responsibilities

The Principal Investigator's primary responsibilities include:

  • Safeguarding the rights and welfare of human subjects throughout clinical trials.
  • Overseeing the study team to ensure compliance with protocols, Good Clinical Practice (GCP), and federal regulations.
  • Maintaining the integrity and accuracy of data collected during trials.
  • Ensuring adherence to Standard Operating Procedures (SOPs), GCPs, and ICH guidelines.
Specific Duties
  • Participate in site initiation visits and training for all active protocols.
  • Maintain current medical licensure and complete necessary SOP training.
  • Provide comprehensive oversight and guidance to the clinical team.
  • Assist in the recruitment process for clinical trials.
  • Conduct informed consent processes in accordance with SOPs.
  • Evaluate patient eligibility for trial inclusion and document all relevant medical histories.
  • Review laboratory results and assess any abnormal findings.
  • Document all clinical trial activities and ensure accurate record-keeping.
  • Report serious adverse events to the sponsor and Institutional Review Board (IRB).
Education and Experience

A qualified individual in the healthcare field (MD) with at least 3 years of clinical research experience is required.

Competencies
  • Exceptional communication and problem-solving skills.
  • Strong organizational and planning abilities.
  • Commitment to customer service excellence.
Technical Skills

In-depth knowledge of FDA-GCP regulations and ethical considerations in clinical research is essential.

Physical and Environmental Requirements

Work is typically performed in a clinical/office environment, with potential for night and weekend hours. Ability to lift up to 20 pounds may be required.

About ACRS Holdings

ACRS Holdings is committed to enhancing the quality of life for individuals through scientific research. We focus on improving efficiencies in clinical trials to overcome challenges in patient recruitment and trial complexity.



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