Clinical Trials - PI - Physician (MD/DO)

Headlands Research; Colorado Springs (CO); On-site; USD 120,000 - 200,000; Part time

Job summary

Headlands Research is seeking a Clinical Trials - PI - Physician (MD/DO) to join their team in Colorado Springs. The role involves overseeing clinical trials, leading diverse teams, and ensuring compliance with ethical guidelines. Ideal candidates are experienced in clinical research with strong leadership skills and a commitment to improving patient outcomes.

Benefits

Flexible Schedule

Dynamic Team Environment

Qualifications

• Previous experience as a Principal Investigator or Sub-Investigator for clinical research trials preferred.
• Active and unencumbered physician license required.
• Excellent communication and leadership skills.

Responsibilities

• Lead and oversee clinical trials ensuring compliance with protocols.
• Provide leadership and mentorship to site staff.
• Communicate effectively with stakeholders including sponsors and research teams.

Skills

Communication

Leadership

Organizational skills

Education

MD or DO license in New Mexico

Board-certified or board-eligible

Job description

Clinical Trials - PI - Physician (MD/DO)

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Clinical Trials - PI - Physician (MD/DO)

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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 Colorado Springs 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 : This role is flexible based on the specific opportunity and needs of the investigator. It can be a part-time role leading into full-time, or permanently part-time with the support of other investigators.
• 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.
  
  

Apply Today

We're an equal-opportunity employer and welcome applicants from all backgrounds and experiences.

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.
  
  

Qualifications

• Previous experience as a Principal Investigator or Sub-Investigator for clinical research trials preferred.
• 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.

Seniority level

• Seniority level

  Mid-Senior level

Employment type

• Employment type

  Part-time

Job function

• Job function

  Health Care Provider

• Industries

  Research Services

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