Hawthorne Health, Inc.
Sub Investigator (NP/PA-C)
Hawthorne Health, Inc., Horsham, Pennsylvania, United States, 19044
3 days ago Be among the first 25 applicants
Hawthorne Health, Inc. provided pay range This range is provided by Hawthorne Health, Inc.. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.
Base pay range $150.00/hr - $160.00/hr
Hawthorne Health is the leading community site network, with 50+ sites across the U.S. and leveraging intelligent technology to accelerate patient access, improve retention, and reduce study costs. By embedding high-quality, compliant research within local communities, Hawthorne makes clinical trials more accessible and convenient for patients. Traditional trial sites are often fragmented and inefficient. Hawthorne streamlines the process by making trials scalable, cost-effective, and patient‑centric. By bringing research directly into communities, Hawthorne shortens timelines and helps bring better treatments to market, faster.
Responsibilities
Assist the Principal Investigator (PI) in overseeing and managing clinical trials conducted at the research site, ensuring adherence to the study protocol, Good Clinical Practice (GCP), ICH guidelines, and all applicable regulatory requirements
Provide medical oversight and ensure the safety and well‑being of study participants throughout the trial, under the supervision of the PI
Perform delegated study‑related duties as assigned by the PI, which may include comprehensive patient assessments, physical exams, medical histories, and eligibility screenings
Review and interpret eligibility, laboratory results, ECGs, and other diagnostic tests as required by the protocol and under PI supervision
Assist the PI in making 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 the PI, study team, and, as delegated, with sponsors, Contract Research Organizations (CROs), Institutional Review Boards (IRBs), and regulatory authorities
Assist with investigational product accountability, storage, and administration according to protocol
Participate in site initiation visits, monitoring visits, audits, and inspections as required
Maintain continuous medical education and stay current with advancements in clinical research and relevant therapeutic areas
Requirements
Must be a NP or PA‑C able to work with adult and pediatric patients
Experience working on at least 3 sponsor initiated clinical trials as a Sub Investigator
Demonstrated knowledge of ICH‑GCP guidelines, FDA regulations, and other relevant ethical and regulatory requirements for clinical research
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
Ability to prioritize tasks and manage time efficiently
Familiarity with clinical trial management systems (CTMS) and electronic data capture (EDC) systems is a plus
Commitment to ethical conduct and patient safety
This position requires coming on site to Horsham, PA site location two times per week.
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.
This is a 1099 contract position.
Seniority level Not Applicable
Employment type Full‑time
Job function Other, Information Technology, and Management
Industries Transportation, Logistics, Supply Chain and Storage
Referrals increase your chances of interviewing at Hawthorne Health, Inc. by 2x
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Hawthorne Health, Inc. provided pay range This range is provided by Hawthorne Health, Inc.. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.
Base pay range $150.00/hr - $160.00/hr
Hawthorne Health is the leading community site network, with 50+ sites across the U.S. and leveraging intelligent technology to accelerate patient access, improve retention, and reduce study costs. By embedding high-quality, compliant research within local communities, Hawthorne makes clinical trials more accessible and convenient for patients. Traditional trial sites are often fragmented and inefficient. Hawthorne streamlines the process by making trials scalable, cost-effective, and patient‑centric. By bringing research directly into communities, Hawthorne shortens timelines and helps bring better treatments to market, faster.
Responsibilities
Assist the Principal Investigator (PI) in overseeing and managing clinical trials conducted at the research site, ensuring adherence to the study protocol, Good Clinical Practice (GCP), ICH guidelines, and all applicable regulatory requirements
Provide medical oversight and ensure the safety and well‑being of study participants throughout the trial, under the supervision of the PI
Perform delegated study‑related duties as assigned by the PI, which may include comprehensive patient assessments, physical exams, medical histories, and eligibility screenings
Review and interpret eligibility, laboratory results, ECGs, and other diagnostic tests as required by the protocol and under PI supervision
Assist the PI in making 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 the PI, study team, and, as delegated, with sponsors, Contract Research Organizations (CROs), Institutional Review Boards (IRBs), and regulatory authorities
Assist with investigational product accountability, storage, and administration according to protocol
Participate in site initiation visits, monitoring visits, audits, and inspections as required
Maintain continuous medical education and stay current with advancements in clinical research and relevant therapeutic areas
Requirements
Must be a NP or PA‑C able to work with adult and pediatric patients
Experience working on at least 3 sponsor initiated clinical trials as a Sub Investigator
Demonstrated knowledge of ICH‑GCP guidelines, FDA regulations, and other relevant ethical and regulatory requirements for clinical research
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
Ability to prioritize tasks and manage time efficiently
Familiarity with clinical trial management systems (CTMS) and electronic data capture (EDC) systems is a plus
Commitment to ethical conduct and patient safety
This position requires coming on site to Horsham, PA site location two times per week.
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.
This is a 1099 contract position.
Seniority level Not Applicable
Employment type Full‑time
Job function Other, Information Technology, and Management
Industries Transportation, Logistics, Supply Chain and Storage
Referrals increase your chances of interviewing at Hawthorne Health, Inc. by 2x
#J-18808-Ljbffr