Job Description

We are seeking a skilled and experienced Medical Physician to join our team as a Principal Investigator at a clinical research site in Las Vegas, Nevada. The primary focus is the oversight of all clinical trial studies according to study protocols, company processes and GCP.

Job Responsibilities

You will ensure the health and safety of participants throughout the study.
Supervise site staff to ensure the implementation of safe and effective trial procedures.
Review and report on screening failures, safety concerns, and participant retention statistics.
Oversee the clinical evaluation and assessment processes within clinical trials.
Maintain regular communication with IRBs and study sponsors.
Adhere to all medical responsibilities as outlined in study protocols, SOPs, GCP, and relevant state regulations.
Gather and analyze data to identify trends and patterns within clinical trial results.
Prepare comprehensive reports detailing findings and suggestions for improvements.
Stay informed on the latest updates in SOPs and documentation standards.
This is a part-time role with flexible hours, ranging from 20-30 hours per week. The schedule will vary based on the clinical trial's requirements, providing adaptability and the chance to contribute to a dynamic and engaging research project

Job Requirements

A minimum of 2 years of experience as a Principal Investigator or Sub-Investigator is preferred
Strong analytical abilities with expertise in collecting, analyzing, and interpreting complex data.
Exceptional written and verbal communication skills, particularly in report writing and presenting findings.
Proven ability to lead a team effectively and manage multiple priorities in a fast-paced environment.
High attention to detail and the ability to handle sensitive information with confidentiality. If you are a motivated individual with a passion for clinical research, we encourage you to apply for this opportunity.

License

Nevada MD License (Required)

Job Tags

Part time, Flexible hours,

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