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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 Aug 10, 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 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.

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 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.
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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 6% As Needed, 62% Full Time, 19% Part Time, and 13% Contract. Highlights an 69% In-person, and 31% Remote job distribution, with an average salary of $151,807 per year, or $73 per hour.

Physician - Clinical Trials - MD/DO

Headlands Research

Albuquerque, NM

Full-time, Part-time

Re-posted 25 days ago

Job description

Join Us in Improving Lives through Clinical Research

At Headlands Research, we're not just building a clinical trial network; we are working to bring clinical trials to underserved communities and new treatments to market. Picture this: an exceptional family of next-generation clinical trial sites, where cutting-edge technology meets unparalleled support services, and participant engagement reaches new heights. Established in 2018, we've rapidly grown to operate 20+ clinical trial sites across the US and Canada, with ambitious plans for expansion on the horizon. 

Championing Diversity in Clinical Trials

Diversity isn't just a checkbox for us-it's central to our mission. We're committed to advancing medical science by promoting diversity in every facet of clinical trial research. From our team composition to participant demographics, inclusivity is at the heart of everything we do.

The Role of a Lifetime

Are you ready to make a difference? We're seeking an experienced Principal Investigator or Sub-Investigator to help us grow a new clinical research site in the Albuquerque area. Whether you're a seasoned Family Medicine physician or a specialist in Endocrinology, Neurology, or other area of medicine, your passion for improving patient outcomes is what matters most. If you have previous experience as an Investigator for clinical research trials, we want to talk with you. We're flexible-we're open to part-time or full-time commitments with flexible schedules.

Why Join Us?

  • Flexible Schedule: Work on your terms, with a schedule that fits your life.
  • Unlimited Potential: The sky's the limit. We're open to up to 40 hours per week, allowing you to maximize your impact.
  • Dynamic Team Environment: You'll help Headlands Research build a diverse and talented team of clinical research coordinators, research assistants, physicians, advanced providers, and patient recruitment specialists. With ample support and a culture of collaboration, you'll thrive in an environment where your contributions truly make a difference. A high level of professionalism is a key differentiator at Headlands.

Responsibilities:

  • Lead and oversee clinical trials conducted at Headlands Research sites, ensuring compliance with protocol requirements, regulatory standards, and ethical guidelines.
  • Provide leadership and mentorship to site staff, fostering a culture of inclusivity, diversity, and professionalism within the research team.
  • Participate in investigator meetings and educational initiatives to stay updated on advancements in clinical research and diversity initiatives.
  • Obtain IRB approval for study initiation and any protocol modifications.
  • Oversee subject safety, trial conduct compliance, and the informed consent process.
  • Communicate effectively with stakeholders including sponsors, monitors, regulators, and research network leadership.
  • Provide ongoing training and support to research staff.

Requirements:

  • Previous experience as a Principal Investigator or Sub-Investigator for clinical research trials required.
  • Active and unencumbered license to practice as an MD or DO within the state of New Mexico required.
  • Must be board-certified or board-eligible.
  • Excellent communication and leadership skills, with the ability to collaborate effectively with sponsors, research teams, and external stakeholders.
  • Familiarity with regulatory requirements, Good Clinical Practice (GCP) guidelines, and industry best practices in clinical research.
  • Strong organizational skills and attention to detail, with the ability to manage multiple projects simultaneously in a fast-paced environment.

Apply