Sub Investigator (NP/PA-C) - Full-Time, 4-6 Week Contract (Concord, NC)

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.nbsp;/divdivbr/divdivbAbout the Role/b/divdivHawthorne Health is seeking a bNurse Practitioner (NP) or Certified Physicians Assistant (PA-C) /bwith experience supporting bsponsor/industry initiated trials /bas a Principal or Sub-Investigator tob lead an upcoming vaccine trial at our site in Concord, NC./b/divbr/br/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 a Nurse Practitioner (NP) or Certified Physicians Assistant (PA-C) with experience supporting sponsor/industry initiated trials as a Principal or Sub-Investigator to lead an upcoming vaccine trial at our site in Concord, NC.
br/br/divThis is a fully on site position./divdivUp to 40 hours a week, temporary position (4-6 week contract)./divbr/br/bResponsibilities/bbr/liAssist 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./liliProvide medical oversight and ensure the safety and well-being of study participants throughout the trial, under the supervision of the PI./liliPerform delegated study-related duties as assigned by the PI, which may include comprehensive patient assessments, physical exams, medical histories, and eligibility screenings./liliReview and interpret eligibility, laboratory results, ECGs, and other diagnostic tests as required by the protocol and under PI supervision./liliAssist the PI in making medical decisions regarding participant care, adverse events, and protocol deviations./liliEnsure accurate, complete, and timely collection and documentation of all study data./liliCommunicate effectively with the PI, study team, and, as delegated, with sponsors, Contract Research Organizations (CROs), Institutional Review Boards (IRBs), and regulatory authorities./liliAssist with investigational product accountability, storage, and administration according to protocol./liliParticipate in site initiation visits, monitoring visits, audits, and inspections as required./liliMaintain continuous medical education and stay current with advancements in clinical research and relevant therapeutic areas./libr/br/bRequirements/bbr/liMust be a NP or PA-C able to work with adult and pediatric patients./liliExperience working on at least 3 sponsor initiated clinical trials as a Sub Investigator./liliDemonstrated knowledge of ICH-GCP guidelines, FDA regulations, and other relevant ethical and regulatory requirements for clinical research./liliStrong interpersonal and communication skills, with the ability to work effectively as part of a team./liliExcellent clinical judgment and problem-solving abilities./liliMeticulous attention to detail and strong organizational skills./liliAbility to prioritize tasks and manage time efficiently./liliFamiliarity with clinical trial management systems (CTMS) and electronic data capture (EDC) systems is a plus./liliCommitment to ethical conduct and patient safety./libr/br/divThis is a strong opportunity for an experienced Sub-Investigator who enjoys being hands-on at the site level. Over a focused b4–6 week contract/b, up to 40 hours a week, you’ll partner closely with our team in Hawthorne Health's innovative, pharmacy-embedded model—supporting study execution, participant safety, and high-quality trial conduct in a community-based setting./div
divbAbout Us/bnbsp;/divdivHawthorne 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.nbsp;/divdivbr/divdivbAbout the Role/b/divdivHawthorne Health is seeking a bNurse Practitioner (NP) or Certified Physicians Assistant (PA-C) /bwith experience supporting bsponsor/industry initiated trials /bas a Principal or Sub-Investigator tob lead an upcoming vaccine trial at our site in Concord, NC./b/divbr/br/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 a Nurse Practitioner (NP) or Certified Physicians Assistant (PA-C) with experience supporting sponsor/industry initiated trials as a Principal or Sub-Investigator to lead an upcoming vaccine trial at our site in Concord, NC.
br/br/divThis is a fully on site position./divdivUp to 40 hours a week, temporary position (4-6 week contract)./divbr/br/bResponsibilities/bbr/liAssist 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./liliProvide medical oversight and ensure the safety and well-being of study participants throughout the trial, under the supervision of the PI./liliPerform delegated study-related duties as assigned by the PI, which may include comprehensive patient assessments, physical exams, medical histories, and eligibility screenings./liliReview and interpret eligibility, laboratory results, ECGs, and other diagnostic tests as required by the protocol and under PI supervision./liliAssist the PI in making medical decisions regarding participant care, adverse events, and protocol deviations./liliEnsure accurate, complete, and timely collection and documentation of all study data./liliCommunicate effectively with the PI, study team, and, as delegated, with sponsors, Contract Research Organizations (CROs), Institutional Review Boards (IRBs), and regulatory authorities./liliAssist with investigational product accountability, storage, and administration according to protocol./liliParticipate in site initiation visits, monitoring visits, audits, and inspections as required./liliMaintain continuous medical education and stay current with advancements in clinical research and relevant therapeutic areas./libr/br/bRequirements/bbr/liMust be a NP or PA-C able to work with adult and pediatric patients./liliExperience working on at least 3 sponsor initiated clinical trials as a Sub Investigator./liliDemonstrated knowledge of ICH-GCP guidelines, FDA regulations, and other relevant ethical and regulatory requirements for clinical research./liliStrong interpersonal and communication skills, with the ability to work effectively as part of a team./liliExcellent clinical judgment and problem-solving abilities./liliMeticulous attention to detail and strong organizational skills./liliAbility to prioritize tasks and manage time efficiently./liliFamiliarity with clinical trial management systems (CTMS) and electronic data capture (EDC) systems is a plus./liliCommitment to ethical conduct and patient safety./libr/br/divThis is a strong opportunity for an experienced Sub-Investigator who enjoys being hands-on at the site level. Over a focused b4–6 week contract/b, up to 40 hours a week, you’ll partner closely with our team in Hawthorne Health's innovative, pharmacy-embedded model—supporting study execution, participant safety, and high-quality trial conduct in a community-based setting./div