Principal Investigator (MD/DO) - Dermatology Clinical Trials

Hawthorne Health, Inc.; Springfield (MO); Hybrid; USD 207,000 - 317,000; Part time

Job summary

Hawthorne Health, Inc. seeks an experienced Principal Investigator (MD/DO) to lead dermatology trials within our community-based site network. This part-time, 1099 role requires on-site presence for key visits (approx.

twice to four times per month) with remote oversight (3–5 hours weekly). You will supervise a site team and ensure adherence to GCP, FDA regulations, and study protocol. The ideal candidate has led at least three sponsor-initiated trials as PI or Sub-I, holds an unrestricted

Qualifications

• Must be an MD with experience leading at least three sponsor-initiated trials as a PI or Sub-I.
• Current, unrestricted medical license.
• Experience with Dermatology indications in clinical trials and/or in a clinical setting.
• Demonstrated knowledge of ICH-GCP guidelines, FDA regulations, and regulatory requirements for clinical research.
• Proven leadership and team management skills.
• Excellent clinical judgment and decision-making abilities.

Responsibilities

• Accurately document findings and contribute to ongoing clinical trials, registries, or research protocols as applicable.
• Oversee and manage all aspects of clinical trials conducted at the research site, ensuring adherence to protocol, GCP, ICH guidelines, and regulatory requirements.
• Lead and supervise the clinical research team, including sub-investigators, study coordinators, and site staff.
• Delegate duties to qualified personnel and ensure proper training and oversight.
• Conduct remote review of patient assessments to ensure appropriate participant enrollment.
• Review laboratory results, ECGs, and diagnostic tests.
• Make critical medical decisions regarding participant care, adverse events, and protocol deviations.
• Ensure accurate, complete, and timely collection and documentation of study data.
• Communicate with sponsors, CROs, IRBs, and regulatory authorities.
• Manage investigational product accountability, storage, and administration per protocol.
• Participate in site initiation visits, monitoring visits, audits, and inspections.
• Maintain continuous medical education and stay current with advancements in clinical research.

Skills

Leadership

Clinical judgment

Communication

GCP/FDA knowledge

Education

MD/DO

Job description

About Us

Hawthorne Health is a leading community site network and home research visit solution provider, with 20+ sites and more than 2,000 research experienced healthcare professionals across the U.S. Hawthorne leverages convenient, trusted, healthcare locations, identified patient data, and intelligent technology to accelerate patient access, improve retention, and reduce study costs. By embedding high-quality research within local communities, Hawthorne makes clinical trials more accessible and convenient for patients. Our community-based model shortens timelines and helps bring better treatments to market, faster.

About The Role

Hawthorne Health is seeking an experienced Principal investigator (MD/DO) for a part-time, 1099 role. Candidates should have prior experience as a PI or Sub-I on sponsor-initiated clinical trials. This role will lead Dermatology trials within our growing, community-based site network—built to make research efficient, patient-friendly, and investigator-supported.

Responsibilities

• Accurately document findings and contribute to ongoing clinical trials, registries, or research protocols as applicable
• Oversee and manage all aspects of clinical trials conducted at the research site, ensuring adherence to the study protocol, Good Clinical Practice (GCP), ICH guidelines, and all applicable regulatory requirements
• Lead and supervise the clinical research team, including sub-investigators, study coordinators, and other site staff
• Delegate study-related duties appropriately to qualified personnel and ensure proper training and oversight
• Conduct remote review of patient assessments, including physical exams, medical histories, and eligibility screenings, to ensure appropriate participant enrollment
• Review and interpret laboratory results, ECGs, and other diagnostic tests
• Make critical medical decisions regarding participant care, adverse events, and protocol deviations
• Ensure accurate, complete, and timely collection and documentation of all study data
• Communicate effectively with sponsors, Contract Research Organizations (CROs), Institutional Review Boards (IRBs), and regulatory authorities
• Manage investigational product accountability, storage, and administration according to protocol and with the help of the on-site IP team
• Participate in site initiation visits, monitoring visits, audits, and inspections
• Maintain continuous medical education and stay current with advancements in clinical research and relevant therapeutic areas

Requirements

• Must be an MD with experience leading at least three sponsor initiated trials as a PI or Sub-I
• Current, unrestricted medical license
• Experience with Dermatology indications in clinical trials and/or in a clinical setting
• Demonstrated in-depth knowledge of ICH-GCP guidelines, FDA regulations, and other relevant ethical and regulatory requirements for clinical research
• Proven leadership and team management skills
• Excellent clinical judgment and decision-making abilities
• Strong verbal and written communication skills in English, with the ability to present complex information clearly and concisely
• Exceptional organizational skills and meticulous attention to detail
• Ability to manage multiple complex studies simultaneously and prioritize tasks effectively
• Commitment to ethical conduct and patient safety

Location

• This role requires on-site presence approximately twice to four times per month for key visits (or more, depending on study needs), with additional oversight responsibilities performed remotely (approximately 3–5 hours per week)
• Preference is for Investigator to live within 1.5 hours driving distance of the site.

Hawthorne Health is transforming the clinical trial landscape through an innovative site model that integrates research into community-based settings like local pharmacies. By meeting patients where they already receive care, we are improving access, strengthening trust, and driving more inclusive and efficient trials.

We welcome the opportunity to connect with individuals interested in being part of this evolving model.

We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us. To view our privacy policy and terms of use, please use the links below. Privacy Policy: https://hawthornehealth.com/privacy-policy/ Terms of Use: https://hawthornehealth.com/terms-of-use/

This is a 1099 independent contractor opportunity. Compensation may be flexible and adjusted based on experience and qualifications.