MD/DO Consultant - Principal Investigator, Clinical Trials

Hawthorne Health; McAllen (TX); Hybrid; USD 138.000 - 344.000; Teilzeit

Zusammenfassung

Hawthorne Health is seeking a Principal Investigator (MD) for a 1099 contract to lead the investigation at our McAllen, TX site. Role requires on-site presence ~1–4 times monthly with 3–5 hours of remote clinical oversight weekly.

Candidate must have at least 3 sponsor-initiated trials, an active medical license, and MD degree. Strong leadership, regulatory knowledge, and excellent communication are essential for compliant trial conduct.

Qualifikationen

• Experience as a Principal Investigator on at least 3 sponsor initiated clinical trials.
• MD degree from an accredited institution.
• Current, unrestricted medical license.
• Board certification in a relevant specialty preferred.
• Demonstrated knowledge of ICH-GCP, FDA regulations, and regulatory requirements.
• Proven leadership and team management skills.
• Excellent clinical judgment and decision-making abilities.
• Strong English communication, both verbal and written.
• Organizational skills and meticulous attention to detail.
• Ability to manage multiple complex studies and prioritize tasks.

Aufgaben

• Accurately document findings and contribute to clinical trials, registries, or research protocols.
• Oversee and manage all aspects of clinical trials at the site, ensuring adherence to protocol and regulatory standards.
• Lead and supervise the clinical research team and delegate duties as needed.
• Conduct remote reviews of patient assessments to ensure proper enrollment.
• Review and interpret laboratory results, ECGs, and diagnostics.
• Make critical medical decisions regarding participant care and protocol deviations.
• Ensure complete and timely data collection and documentation.
• Communicate with sponsors, CROs, IRBs, and regulators.
• Manage investigational product accountability and IP team collaboration.
• Participate in site initiation, monitoring visits, audits, and inspections.
• Maintain ongoing medical education and stay current with research advances.

Kenntnisse

PI leadership

Team management

Regulatory knowledge

Clinical judgment

English communication

Ausbildung

MD degree (M.D.)

Medical license

Board certification preferred

Jobbeschreibung

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 on a 1099 contract opportunity to join our growing team and lead the investigation for our new site in McAllen, TX.

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

• Experience as a Principal Investigator on at least 3 sponsor initiated clinical trials.
• Medical Doctor (M.D. or equivalent) degree from an accredited institution.
• Current, unrestricted medical license.
• Board certification in a relevant specialty preferred.
• 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 & Time Commitment

• 3-5 hours per week of remote clinical oversight.
• This position requires being on site in McAllen, TX ~1-4 times per month for key visits.
• PI will need to be located within 1.5 hours driving distance to the site.

$100 - $250 an hour

Position Type: Part-time, 1099 contract

Compensation: Hourly; rate negotiable based on experience

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 mode