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Clinical Research Trials Jobs (NOW HIRING)

DaVinci Research

Clinical Research Coordinator

Roseville, CA · On-site

$25.50 - $33.75/hr

Company Description DaVinci Research (DVR) is a leading Site Management Organization dedicated to conducting clinical research trials. In collaboration with innovative pharmaceutical and medical ...

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Clinical Research Trials information

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$49K

$107.3K

$189K

How much do clinical research trials jobs pay per year?

As of Jul 20, 2026, the average yearly pay for clinical research trials in the United States is $107,336.00, according to ZipRecruiter salary data. Most workers in this role earn between $81,000.00 and $122,500.00 per year, depending on experience, location, and employer.

What are clinical research trials?

Clinical research trials, also known as clinical trials, are research studies conducted with human volunteers to evaluate the safety and effectiveness of new medical treatments, drugs, devices, or interventions. These trials follow strict scientific and ethical guidelines to ensure the well-being of participants and to generate reliable data. Clinical trials are essential for advancing medical knowledge and for regulatory approval of new therapies before they become widely available to the public.

What are the key skills and qualifications needed to thrive in Clinical Research Trials, and why are they important?

To thrive in Clinical Research Trials, you need a solid understanding of clinical protocols, regulatory guidelines (such as GCP), and often a degree in life sciences or a related field. Familiarity with electronic data capture (EDC) systems, clinical trial management software, and relevant certifications like CCRA or CCRP are highly valuable. Strong organizational skills, attention to detail, and effective communication are essential soft skills for coordinating with multidisciplinary teams and ensuring protocol compliance. Mastery of these skills is crucial for maintaining data integrity, patient safety, and the overall success of research studies.

What are some common challenges faced by professionals working in clinical research trials and how can they be addressed?

Professionals in clinical research trials often encounter challenges such as patient recruitment, ensuring protocol compliance, and managing complex regulatory requirements. Recruitment can be improved by building strong relationships with referring physicians and patient communities. Maintaining protocol compliance requires thorough training and regular communication with study sites. Staying updated on regulations and leveraging electronic data management systems can help streamline documentation and reporting. Collaboration with cross-functional teams, like data managers and regulatory specialists, is key to overcoming these challenges and ensuring successful trial outcomes.

What is the difference between Clinical Research Trials vs Clinical Research Coordinators?

AspectClinical Research Trials

Clinical Research Trials are the actual studies conducted to evaluate new medical treatments, involving protocol development, data collection, and analysis. They are typically led by principal investigators and involve multiple team members. Clinical Research Coordinators (CRCs) are professionals who manage the day-to-day operations of these trials, including patient recruitment, data entry, and regulatory compliance. Both roles require knowledge of clinical protocols and certifications like CCRC or CCRP. While Clinical Research Trials refer to the studies themselves, CRCs are key personnel executing these studies in healthcare settings.

More about Clinical Research Trials jobs
What cities are hiring for Clinical Research Trials jobs? Cities with the most Clinical Research Trials job openings:
What states have the most Clinical Research Trials jobs? States with the most job openings for Clinical Research Trials jobs include:
What job categories do people searching Clinical Research Trials jobs look for? The top searched job categories for Clinical Research Trials jobs are:
Clinical Research Trials jobs near you
Infographic showing various Clinical Research Trials job openings in the United States as of July 2026, with employment types broken down into 3% As Needed, 72% Full Time, 18% Part Time, and 7% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $107,336 per year, or $51.6 per hour.
Physician - Clinical Trials - MD/DO

Physician - Clinical Trials - MD/DO

Headlands Research

Little Rock, AR

Other

Re-posted 5 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 Little Rock 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 Arkansas 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