Clinical Trials - PI - Physician (MD/DO)

Headlands Research, Inc.; Colorado Springs (CO); On-site; USD 80,000 - 150,000; Part time

Job summary

An innovative clinical research organization is seeking a Principal Investigator or Sub-Investigator to establish a new site in Colorado Springs. This role offers flexibility with part-time or full-time options, allowing you to adapt your schedule to meet personal needs. You will lead clinical trials, ensuring compliance with ethical standards while mentoring a diverse team of professionals. This position provides a unique opportunity to contribute to meaningful clinical research that impacts underserved communities. Join a dynamic team committed to inclusivity and excellence in clinical trials.

Benefits

Flexible Schedule

Dynamic Team Environment

Qualifications

• Experience as a Principal or Sub-Investigator preferred.
• Active MD or DO license in New Mexico required.

Responsibilities

• Lead clinical trials, ensuring compliance with protocols and regulations.
• Mentor and lead site staff, fostering inclusivity and professionalism.

Skills

Leadership Skills

Communication Skills

Organizational Skills

Knowledge of Regulatory Standards

Clinical Research Experience

Education

MD or DO License

Board Certification

Job description

Overview

Join Us in Improving Lives through Clinical Research

At Headlands Research, we're building a clinical trial network focused on bringing trials to underserved communities and introducing new treatments. We operate over 20 clinical trial sites across the US and Canada, with plans for expansion.

Championing Diversity in Clinical Trials

Diversity is central to our mission, reflected in our team and participant demographics, promoting inclusivity in clinical research.

The Role of a Lifetime

We seek an experienced Principal Investigator or Sub-Investigator to help establish a new site in Colorado Springs. Relevant medical specialties include Family Medicine, Endocrinology, Neurology, or others. Previous clinical research experience is required. We offer flexible, part-time or full-time roles.

Why Join Us?

• Flexible Schedule: Adaptable based on the investigator's needs, including part-time or full-time roles.
• Dynamic Team Environment: Collaborate with a diverse team of research professionals in a supportive, professional setting.

Apply Today

We are an equal-opportunity employer welcoming applicants from all backgrounds.

Responsibilities

• Lead clinical trials, ensuring compliance with protocols, regulations, and ethics.
• Mentor and lead site staff, fostering inclusivity and professionalism.
• Participate in meetings and educational initiatives to stay current.
• Obtain IRB approval for studies and modifications.
• Oversee subject safety, trial conduct, and consent processes.
• Communicate with sponsors, monitors, regulators, and leadership.
• Provide training and support to research staff.

Qualifications

• Experience as a Principal or Sub-Investigator preferred.
• Active MD or DO license in New Mexico required.
• Board-certified or eligible.
• Strong communication, leadership, and organizational skills.
• Knowledge of regulatory standards and GCP guidelines.