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Physician - Clinical Trials - MD​/DO Milwaukee, WI

Job in Milwaukee, Milwaukee County, Wisconsin, 53244, USA
Listing for: Headlands Research, Inc.
Full Time, Part Time position
Listed on 2025-12-02
Job specializations:
  • Doctor/Physician
    Medical Doctor
Job Description & How to Apply Below

Overview

At Headlands Research, we are dedicated to enhancing clinical trial delivery within our communities. As a leading network of advanced clinical trial sites, we leverage cutting-edge technology and exceptional support services to broaden outreach and participation. Founded in 2018, our rapidly growing company currently operates 20+ sites across the US and Canada, with plans for further expansion.

Join Us in Improving Lives through Clinical Research

We are not just building a clinical trial network; we are working to bring clinical trials to underserved communities and new treatments to market. Picture 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 is central to our mission. We are 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

The Role of a Lifetime

We are seeking an experienced Principal Investigator or Sub-Investigator to help us grow a new clinical research site in the Milwaukee area. Whether you are a seasoned Family Medicine physician or a specialist in Endocrinology, Neurology, or another area of medicine, your passion for improving patient outcomes is what matters most. If you have prior experience as an Investigator for clinical research trials, we want to talk with you.

We are flexible—we are 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 are 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 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 required.
  • Active and unencumbered license to practice as an MD or DO within the state of Wisconsin required.
  • 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.
Voluntary Self-Identification

For government reporting purposes, we ask candidates to respond to the below self-identification survey. Completion of the form is entirely voluntary. Whatever your decision, it will not be considered in the hiring process or thereafter. Any information you provide will be…

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