Principal Investigator (Rheumatology)

Be Well Clinical Studies • Lincoln, NE

4d • $20,000 - $100,000 • Onsite

About The Position

Be Well Clinical Studies is seeking experienced and specialized physicians to serve as independent contractor Principal Investigators (PIs) for clinical research studies. Our mission is to advance medical science by conducting high-quality clinical trials that bring innovative treatments to patients. This is a 1099 contracted role and not a position of employment. As an independent PI contractor, you will be responsible for the ethical, compliant, and efficient oversight of clinical trials. You will ensure subject safety, protocol adherence, and data integrity, while collaborating with research teams and sponsors. Compensation is paid per study, with earnings typically ranging from $20,000 to $100,000 depending on study complexity and volume. Potential dermatological studies may include: Rheumatoid Arthritis Osteoarthritis Psoriatic Arthritis Lupus Gout Ankylosing Spondylitis Why Contract With Us? • Flexible, part-time commitment that complements your current practice. • Competitive compensation structure for each contracted study. • Opportunity to contribute to groundbreaking treatments and advancements in medicine. Note: This opportunity is offered strictly as a 1099 independent contractor engagement. You will not be classified as an employee of Be Well Clinical Studies and will be responsible for your own taxes, liability coverage, and applicable business expenses.

Requirements

• MD or DO with an active, unrestricted medical license.
• Clinical research experience preferred (PI training available if needed).
• Strong organizational and communication skills.
• Availability for approximately 8–10 hours per week, with 4–8 hours on-site in clinic (as study needs dictate).
• Must be responsive for remote consults via text, phone, or Zoom.

Responsibilities

• Study Oversight – Independently manage and lead clinical trials in accordance with FDA, GCP, and IRB/IEC guidelines.
• Patient Safety & Consent – Oversee participant safety, review adverse events, and ensure informed consent processes.
• Data Integrity – Maintain accuracy in study documentation and compliance with protocol-specific requirements.
• Collaboration – Partner with site staff, sponsors, and regulatory monitors to ensure study success.
• Compliance – Uphold all regulatory, ethical, and contractual obligations throughout the duration of the study.

Benefits

• Flexible, part-time commitment that complements your current practice.
• Competitive compensation structure for each contracted study.
• Opportunity to contribute to groundbreaking treatments and advancements in medicine.

What This Job Offers

• Job Type: Part-time
• Career Level: Principal
• Education Level: Ph.D. or professional degree