Rheumatologist - Clinical Research Investigator

ECN Operating LLC; Scottsdale (AZ); On-site; USD 200,000 - 250,000; Part time

Job summary

ECN Operating LLC is looking for a dedicated Physician – Rheumatologist to join our clinical trials team in Scottsdale, Arizona. This part time/per diem role requires overseeing clinical trials as a Principal Investigator, ensuring high-quality medical care for patients while contributing to critical medical research.

The ideal candidate will have a medical degree, a valid medical license, and board certification in Rheumatology. Strong communication and attention to detail are essential for success in this fast-paced environment.

Qualifications

• MD or DO degree required.
• Valid medical license in Arizona.
• Board Certified/Eligible in Rheumatology or Family/Geriatric Medicine.
• Good Clinical Practice certification is preferred.

Responsibilities

• Serve as Principal Investigator on clinical trials.
• Perform physical exams and clinical assessments.
• Evaluate patient eligibility for trials.
• Provide medical oversight for participants.

Skills

Attention to detail

Interpersonal skills

Communication skills

Familiarity with FDA and ICH-GCP

Education

MD or DO degree from an accredited medical school

Valid, unrestricted medical license

Board Certified or Board Eligible in Rheumatology

BC/BE in Family Medicine or Geriatric Medicine

Tools

Electronic medical records (EMRs)

Clinical trial management systems (CTMS)

Job description

Elite Clinical Network (ECN) is seeking a dedicated and research-oriented Physician – Rheumatologist to join our expanding team of clinical professionals. The ideal candidate will play a critical role in the conduct of clinical trials by serving as a Principal Investigator (PI) or Sub-Investigator, while continuing to provide high-quality medical care to adult patients within a clinical research setting. This is a part time/per diem position with a unique opportunity to contribute to the advancement of medicine through clinical studies.

Key Responsibilities

• Serve as Principal Investigator or Sub-Investigator on multiple Phase I–IV clinical trials.
• Perform comprehensive physical exams and clinical assessments for protocol screening and enrollment.
• Evaluate patient eligibility based on inclusion/exclusion criteria of clinical protocols.
• Provide medical oversight for clinical trial participants, including safety assessments, adverse event evaluations, and ongoing care.
• Collaborate closely with Clinical Research Coordinators, Sponsors, and Monitors to ensure protocol compliance and data integrity.
• Review and sign off on source documents, case report forms (CRFs), and regulatory documentation.
• Maintain detailed and accurate clinical trial documentation in compliance with ICH-GCP, FDA, and sponsor requirements.
• Participate in Site Initiation Visits (SIVs), Monitoring Visits, and Audits as needed.
• Manage chronic and acute conditions among study participants in alignment with standard care and protocol guidelines.
• Educate and counsel patients on study procedures, informed consent, and potential side effects.
• Support recruitment efforts and promote patient retention in trials.

Qualifications

• MD or DO degree from an accredited medical school.
• Valid, unrestricted medical license in the state of employment.
• Board Certified or Board Eligible (BC/BE) in Rheumatology.
• BC/BE in Family Medicine or Geriatric Medicine will also be considered.
• Current Good Clinical Practice (GCP) certification or willingness to obtain prior to start.
• Minimum of 1 year of experience in clinical practice; prior clinical research experience preferred but not required.

Preferred Skills

• Familiarity with FDA, ICH-GCP, and clinical trial protocols.
• Experience managing or participating in industry-sponsored clinical trials.
• Strong attention to detail and ability to document accurately.
• Excellent interpersonal and communication skills for patient interaction and sponsor collaboration.
• Ability to work collaboratively with a cross-functional team in a fast-paced research environment.
• Comfortable using electronic medical records (EMRs) and clinical trial management systems (CTMS).