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 initiated trials as a Principal or Sub-Investigator to lead upcoming trials at our site in Springfield, MO. 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
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 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. To view our privacy policy and terms of use, please use the links below. Privacy Policy: https://hawthornehealth.com/privacy-policy/ Terms of Use: https://hawthornehealth.com/terms-of-use/