hero

Work for companies that improve the lives of healthcare professionals and patients

Clinical Research Coordinator

Hawthorne Effect

Hawthorne Effect

Administration
lebanon, tn, usa
Posted on Jan 25, 2026
About Hawthorne Health:
Hawthorne Health is dedicated to advancing clinical research and improving patient outcomes through high-quality, community-based clinical trials. We partner with leading sponsors and investigators to bring innovative therapies to our patients in a compassionate, professional setting.

Position Overview:
Hawthorne Health is seeking an experienced Clinical Research Coordinator (CRC) to join our Lebanon, TN site. The ideal candidate will be detail-oriented, highly organized, and experienced in all aspects of clinical trial coordination. This individual will work closely with investigators, patients, and sponsor representatives to ensure successful execution of clinical trials in compliance with all regulatory and protocol requirements.

Key Responsibilities

  • Conduct and coordinate all aspects of clinical trial activities at the site
  • Perform phlebotomy on both pediatric and adult patients, following proper clinical and safety protocols
  • Recruit, screen, and enroll study participants according to inclusion/exclusion criteria
  • Schedule and conduct study visits, ensuring adherence to protocol requirements
  • Accurately collect, process, and ship biological samples per study-specific guidelines
  • Complete and maintain study documentation, including source documents, regulatory binders, and informed consent forms
  • Perform timely and accurate data entry into electronic data capture systems (EDC)
  • Communicate effectively with sponsors, monitors, and other research team members
  • Ensure compliance with GCP, ICH, FDA, and IRB regulations
  • Assist in monitoring visits and audit preparation as needed



Qualifications

  • Minimum of 1–2 years of experience as a Clinical Research Coordinator role
  • Phlebotomy certification or demonstrated competency in venipuncture (pediatric and adult required)
  • Strong understanding of clinical trial operations, regulatory documentation, and data management
  • Excellent attention to detail, organization, and time management skills
  • Strong interpersonal and communication abilities with patients and clinical staff
  • Proficient in Microsoft Office and electronic data capture systems
  • CPR certification preferred



Location

  • This is a part-time position requiring on-site presence in Lebanon, TN two (2) days per week or approximately 18-24 hours 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.