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Flexible Labcorp Clinical Trials information

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How much do flexible labcorp clinical trials jobs pay per hour?

As of Sep 3, 2026, the average hourly pay for flexible labcorp clinical trials in the United States is $72.98, according to ZipRecruiter salary data. Most workers in this role earn between $59.13 and $74.76 per hour, depending on experience, location, and employer.

What is flexible Labcorp clinical trials?

Flexible Labcorp Clinical Trials are research studies conducted by Labcorp that allow participants to take part in clinical trials with adaptable scheduling and remote or at-home participation options. These trials are designed to make it easier for individuals to contribute to medical research without the need for frequent in-person visits. Participants may complete certain study activities at home, online, or via telemedicine, depending on the specific trial. This flexibility helps improve access and convenience for volunteers while maintaining the integrity of the research.

What does a typical week look like for someone working in a flexible Labcorp clinical trials role?

In a flexible Labcorp Clinical Trials position, your week may involve a mix of remote and on-site work, depending on the specific study requirements and your assigned responsibilities. You may be scheduling and conducting patient visits, ensuring timely data entry, coordinating with clinical research teams, and maintaining compliance with study protocols. Collaboration is key, as you'll regularly communicate with investigators, site staff, and project managers to address challenges and keep trials running smoothly. Flexibility allows you to adapt your schedule to both participant needs and study timelines, making strong organizational skills essential for success.

What are the key skills and qualifications needed to thrive in a flexible Labcorp clinical trials role?

To thrive in a flexible clinical trials role at Labcorp, you generally need a background in life sciences or healthcare, experience with clinical research, and relevant certifications such as GCP (Good Clinical Practice). Familiarity with electronic data capture (EDC) systems, clinical trial management systems (CTMS), and regulatory compliance tools is typically required. Strong organizational skills, attention to detail, and effective communication are crucial soft skills for managing multiple studies and collaborating with cross-functional teams. These competencies are vital for ensuring trials run smoothly, data integrity is maintained, and regulatory standards are met.

What is the difference between Flexible Labcorp Clinical Trials vs Clinical Research Coordinator?

AspectFlexible Labcorp Clinical TrialsClinical Research Coordinator
CredentialsTypically requires a bachelor's degree in health sciences or related fieldRequires a bachelor's degree, often in health sciences or related areas
Work EnvironmentFlexible, often remote or hybrid settings, including clinics and labsPrimarily in clinical settings, hospitals, or research facilities
Employer & IndustryLabcorp, pharmaceutical companies, contract research organizationsHospitals, research institutions, pharmaceutical companies

Flexible Labcorp Clinical Trials roles focus on managing and supporting clinical trial processes with flexible schedules, often remotely. Clinical Research Coordinators handle the day-to-day operations of clinical studies in more traditional, on-site environments. Both roles require similar educational backgrounds but differ mainly in work setting and flexibility.

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Flexible Labcorp Clinical Trials jobs near you
Infographic showing various Flexible Labcorp Clinical Trials job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 67% Full Time, 29% Part Time, and 3% Contract. Highlights an 88% Physical, 1% Hybrid, and 11% Remote job distribution, with an average salary of $151,807 per year, or $73 per hour.

Principal Investigator (MD/DO) - Respiratory Clinical Trials

Hawthorne Health

Lebanon, TN • On-site

$150 - $250/hr

Contractor

Posted 8 days ago

Key responsibilities

  • Accurately document findings and contribute to clinical trials, registries, or research protocols.

  • Oversee and manage all aspects of clinical trials at the research site, ensuring compliance with study protocols and regulatory requirements.

  • Lead and supervise the clinical research team, including delegating duties and ensuring proper training and oversight.

Job description

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/DO) for a part-time, 1099 role. Candidates should have prior experience as a PI or Sub-I on sponsor-initiated clinical trials. This role will lead Respiratory trials including Asthma within our growing, community-based site network—built to make research efficient, patient-friendly, and investigator-supported.
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
  • Must be an MD with experience leading at least three sponsor initiated trials as a PI or Sub-I.
  • Current, unrestricted medical license.
  • Experience with respiratory indications in clinical trials and/or in a clinical setting.
  • 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
  • This role requires on-site presence approximately twice per month for key visits (or more, depending on study needs), with additional oversight responsibilities performed remotely (approximately 3–5 hours per week).
  • Preference is for Investigator to live within 1.5 hours driving distance of the site. 
This is a 1099 independent contractor opportunity. Compensation may be flexible and adjusted based on experience and qualifications.

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.

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/