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Medical In Clinical Trials Jobs in Colorado (NOW HIRING)

ECN Operating LLC

Clinical Research Coordinator

Denver, CO · On-site

$25 - $33.25/hr

Candidates with current Phlebotomy certification or Medical Assistant (MA) certification are ... Experience working in clinical trials, especially in a hospital or academic setting. * Familiarity ...

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Medical In Clinical Trials information

What is the difference between Medical In Clinical Trials vs Clinical Research Coordinator?

AspectMedical In Clinical TrialsClinical Research Coordinator
CredentialsMedical degree or relevant healthcare certificationBachelor's degree, often in health or science fields
Work EnvironmentHospitals, clinics, research centersResearch sites, hospitals, clinics
Employer & IndustryPharmaceutical companies, CROs, academic institutionsResearch organizations, hospitals, clinics
Primary FocusOverseeing patient care and medical procedures in trialsManaging study logistics, data collection, and compliance

Medical In Clinical Trials typically involves direct patient care and medical oversight during clinical studies, requiring healthcare credentials. In contrast, Clinical Research Coordinators focus on managing study operations and data. Both roles are essential in clinical research but differ in responsibilities and qualifications.

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Infographic showing various Medical In Clinical Trials job openings in Colorado as of August 2026, with employment types broken down into 1% As Needed, 78% Full Time, 15% Part Time, and 6% Contract. Highlights an 91% Physical, 1% Hybrid, and 8% Remote job distribution.

Physician - Clinical Trials - MD/DO

Headlands Research

Denver, CO • On-site

Full-time, Part-time

Re-posted 8 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 Denver 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 Colorado 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