ABOUT US:

Be Well Clinical Studies is seeking experienced and specialized physicians to serve as Principal Investigators (PI) in our clinical research studies. Our mission is to advance medical science by conducting high-quality clinical trials that bring innovative treatments to patients.

QUALIFICATIONS:

• MD or DO with an active medical license.
• Experience in clinical research or willingness to complete PI training.
• Strong leadership, communication, and organizational skills.
• Ability to commit at least 8-10 hours per week to oversee trials and engage with study teams.
• Flexibility around current schedule
• Time in clinic 4 to 8 hours per week, more if investigator has time
• Available via text or Zoom for consultations

ROLE OVERVIEW:

As an independent PI Contractor, you will oversee clinical trials, ensuring they are conducted ethically, safely, and in compliance with regulatory guidelines. You will play a crucial role in patient safety, data integrity, and study success.

KEY RESPONSIBILITIES:

• Study Oversight: Lead and manage clinical trials, ensuring compliance with FDA, GCP, and IRB regulations.
• Patient Care & Safety: Monitor patient safety, assess adverse events, and ensure informed consent.
• Data Integrity: Ensure accurate documentation and adherence to study protocols.
• Collaboration: Work with research staff, sponsors, and regulatory bodies to execute trials effectively.
• Regulatory Compliance: Maintain ethical standards and ensure adherence to research guidelines.