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Clinical Trials - PI - Physician (MD/DO)

Headlands Research

Charlotte (NC)

On-site

USD 200,000 - 300,000

Part time

5 days ago
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Job summary

A leading company in clinical research is seeking a Principal Investigator for its Charlotte site. This role emphasizes the importance of diversity and aims to improve patient outcomes through clinical trials. Ideal candidates will have a strong background in clinical research, an MD or DO license, and exceptional leadership skills in a flexible environment.

Benefits

Flexible Schedule
Dynamic Team Environment

Qualifications

  • Active unencumbered MD or DO license required in North Carolina.
  • Board-certified or board-eligible preferred.
  • Experience in clinical trials and regulatory requirements.

Responsibilities

  • Lead and oversee clinical trials ensuring compliance with protocols.
  • Mentor site staff and foster a culture of inclusivity.
  • Obtain IRB approval and manage subject safety.

Skills

Communication
Leadership
Organizational Skills

Education

MD or DO License
Board Certification

Job description

Clinical Trials - PI - Physician (MD/DO)

Join to apply for the Clinical Trials - PI - Physician (MD/DO) role at Headlands Research

Clinical Trials - PI - Physician (MD/DO)

3 days ago Be among the first 25 applicants

Join to apply for the Clinical Trials - PI - Physician (MD/DO) role at Headlands Research

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 Charlotte 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 North Carolina 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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