Physician, MD/DO - Clinical Research

Physician Pivot

Florida

On-site

USD 180,000 - 320,000

Full time

48 hours ago
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Benefits offered by this job

Health insurance
401(k) plan
Paid time off
Company holidays

Job summary

Headlands Research in Lake Worth, FL is seeking an experienced physician to serve as Principal Investigator for vaccine clinical trials at the JEM Research Institute. This onsite, full-time role oversees trials, ensures protocol adherence, and mentors a diverse team of coordinators, staff, and investigators.

The ideal candidate is board-certified/eligible, licensed in Florida, and experienced as PI or Sub-I.

Qualifications

  • Eligible for Florida MD/DO license.
  • Board-certified or board-eligible.
  • Experience as Principal Investigator or Sub-Investigator preferred.
  • Strong leadership and communication skills.

Responsibilities

  • Lead and oversee clinical trials at Headlands Research sites, ensuring protocol, regulatory, and ethical compliance.
  • Provide leadership and mentorship to site staff, fostering inclusivity and professionalism.
  • 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 protocol modifications.
  • Oversee subject safety, trial conduct compliance, and informed consent process.

Skills

Leadership
Communication
Regulatory knowledge
GCP knowledge
IRB experience

Education

MD/DO license in FL

Job description

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.

Location: Lake Worth, FL | Site Name: JEM Headlands LLC | Full‑Time | Clinical 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 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.

Why Join Us?

You’ll be part of a growing, mission‑driven organization that values its people. At our core, we’re committed to bringing innovative medical treatments to patients faster—while creating an environment where employees thrive. If you’re passionate about clinical research and ready to make a difference, we’d love to hear from you.

  • 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 physician to help us grow our clinical research site at JEM Research Institute in Lake Worth, FL primarily physicians with previous experience serving as a Principal Investigator (PI) on vaccine clinical trials.
  • Dynamic Team Environment: You'll help Headlands Research continue to 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 a huge plus, but willing to consider those without.
  • Eligible for or active unencumbered license to practice as an MD or DO within the state of Florida 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.

Type: Regular Full‑time Employee

Schedule: Mondays through Fridays, 8:00am - 5:00pm

Location: Onsite in Lake Worth, FL (no capabilities for remote or hybrid work)

Benefits

Our benefits package for full‑time employees includes health insurance (medical, dental, and vision), Health Savings Accounts (HSA) and Flexible Spending Accounts (FSA), Paid Time Off (PTO), a variety of disability, accident, and life insurance options, as well as many more.

What We Offer
  • Competitive pay + annual performance incentives
  • Medical, dental, and vision insurance
  • 401(k) plan with company match
  • Paid time off (PTO) and company holidays
  • A mission‑driven culture focused on advancing medicine and improving patient outcomes

Headlands Research will never ask a candidate for personal identifiable information (date of birth, social security number, driver’s license information, etc) via email or messenger tools, or for a financial deposit of any kind.

Headlands Research is an Equal Opportunity Employer. We do not discriminate on the basis of race, color, religion, age, sex, national origin, disability status, genetic information, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws.

Need Assistance?

Headlands Research is committed to providing access and reasonable accommodation in its employment for individuals with disabilities. To request disability accommodation in the application process, contact recruiting@headlandsresearch.com for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.

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