SonicJobs Logo
Left arrow iconBack to search

Principal Investigator (MD/DO) – Staten Island, NY

Hawthorne Health
Posted 4 months ago, valid for 14 days
Location

New York, New York 10008, NY

Salary

$250 - $250 per hour

Contract type

Full Time

By applying, a Sonicjobs account will be created for you. Sonicjobs's Privacy Policy and Terms & Conditions will apply.

SonicJobs' Terms & Conditions and Privacy Policy also apply.

Sonic Summary

info
  • Hawthorne Health is seeking a Principal Investigator MD for a 1099 contract opportunity, requiring experience as a Principal Investigator on at least three sponsor-initiated clinical trials.
  • The role involves overseeing clinical trials, managing a research team, and ensuring compliance with regulatory requirements while conducting remote patient assessments.
  • Candidates must possess a Medical Doctor (M.D. or equivalent) degree and a current, unrestricted medical license in New York, with board certification preferred.
  • The position offers a competitive pay rate of $250 per hour, with compensation flexible based on experience and qualifications.
  • The job requires 3-5 hours of remote clinical oversight per week and on-site presence in Staten Island, NY, approximately twice a 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.

\n


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 New York.
  • 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 & Schedule
  • 3-5 hours per week of remote clinical oversight.
  • This position requires being on site in Staten Island, NY for key visits, ~2 times a month. 


\n
$250 - $250 an hour
This is a 1099 independent contractor opportunity, offering a competitive rate of $250 per hour. Compensation may be flexible and adjusted based on experience and qualifications.
\n

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.




Learn more about this Employer on their Career Site

Apply now in a few quick clicks

By applying, a Sonicjobs account will be created for you. Sonicjobs's Privacy Policy and Terms & Conditions will apply.

SonicJobs' Terms & Conditions and Privacy Policy also apply.