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MD/DO Consultant - Principal Investigator - Horsham, PA

Hawthorne Health
Posted 5 months ago, valid for 15 days
Location

Hatboro, Montgomery 19040

Salary

$250 - $250 per hour

Contract type

Full Time

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Sonic Summary

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  • Hawthorne Health is looking for a Principal Investigator MD to join their team on a part-time, 1099 contract basis.
  • The role requires at least 3 years of experience as a Principal Investigator on sponsor-initiated clinical trials and a current, unrestricted medical license in Pennsylvania.
  • Responsibilities include overseeing clinical trials, managing the research team, and ensuring compliance with regulatory requirements.
  • The compensation for this position is $250 per hour, with the opportunity for negotiation based on experience.
  • The role involves 3-5 hours of remote clinical oversight per week and requires on-site presence in Horsham, PA, two days per month.

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 site.

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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 in Pennsylvania.
  • 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
  • 3-5 hours per week of remote clinical oversight.
  • This position requires being on site in Horsham, PA two days per month.


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$250 - $250 an hour
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Additional Details

 

Position Type: Part-time, 1099 contract

Compensation: Hourly; rate negotiable based on experience

 

If you’re interested in a flexible role where your clinical expertise directly expands patient access to research, apply today!




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