Rheumatology Sub-Investigator — Part-Time Clinical Trials

Hawthorne Health, Inc.; Lebanon (TN); Hybrid; USD 96,000 - 165,000; Part time

Job summary

A healthcare organization seeks a Rheumatologist Consultant to join its team part-time in Lebanon, TN. Ideal candidates are MD, NP, or PA-C with rheumatology expertise. Responsibilities include comprehensive patient evaluations, conducting disease assessments, assisting in clinical trials, and ensuring participant safety. Strong communication, clinical judgment, and organizational skills are crucial. This position requires on-site availability 1-2 days per week and offers a unique opportunity to contribute to patient-centered clinical research efforts.

Qualifications

• Must be an MD, NP, or PA-C with experience in rheumatology.
• Strong interpersonal and communication skills, with the ability to work effectively as part of a team.
• Excellent clinical judgment and problem-solving abilities.
• Meticulous attention to detail and strong organizational skills.

Responsibilities

• Perform comprehensive rheumatologic evaluations and manage patients.
• Conduct standardized disease assessments using validated instruments.
• Assist the Principal Investigator in overseeing clinical trials.
• Provide medical oversight ensuring safety of study participants.
• Review and interpret eligibility criteria and diagnostic tests.
• Ensure accurate collection and documentation of study data.

Skills

Strong interpersonal and communication skills

Excellent clinical judgment

Problem-solving abilities

Attention to detail

Organizational skills

Time management

Education

MD, NP, or PA-C with experience in rheumatology

Tools

Clinical trial management systems (CTMS)

Electronic data capture (EDC) systems

Job description

A healthcare organization seeks a Rheumatologist Consultant to join its team part-time in Lebanon, TN. Ideal candidates are MD, NP, or PA-C with rheumatology expertise. Responsibilities include comprehensive patient evaluations, conducting disease assessments, assisting in clinical trials, and ensuring participant safety. Strong communication, clinical judgment, and organizational skills are crucial. This position requires on-site availability 1-2 days per week and offers a unique opportunity to contribute to patient-centered clinical research efforts.