Physician, MD/DO - Clinical Research
Headlands Research
$130 - $150 / hour
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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.
Type: Regular Full-time Employee
Schedule: up to 32 hours per week
Pay Range: $130-150/hr *Dependent upon relevant experience, certification, and education.
Location: Onsite in Sacramento, CA (no capabilities for remote or hybrid work)
Reports to: Regional Director of Operations
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.
The Company
Headlands Research has two research sites providing coverage to the greater Sacramento area in northern California. Our medical director, Jeffrey D. Wayne MD has served as a Principal Investigator since 1992, overseeing more than 300 phase 2, 3 and 4 studies. Headlands Research brings the experience, the team, the facilities, the dedication and the reaction time to positively impact your study enrollment objectives. Our experienced team brings deep expertise across multiple therapeutic areas, including cardiometabolic, endocrine disease, and CNS indications such as pain management, delivering high-quality study execution, strong patient engagement, and compassionate care that supports the advancement of future therapies.
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.
Are you ready to make a difference?
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, 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.
- Current and unencumbered license to practice as an MD or DO within the state of California required (or eligible for).
- 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.
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.
Benefits
- Lead and oversee clinical trials, 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.
- Previous experience as a Principal Investigator or Sub-Investigator for clinical research trials a huge plus, but willing to consider those without.
- Current and unencumbered license to practice as an MD or DO within the state of California required (or eligible for).
- 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.
About this role
Headlands Research operates a network of clinical trial sites across the US and Canada and is seeking a physician to lead trial operations at their Sacramento location. You would oversee study conduct across multiple therapeutic areas—cardiometabolic, endocrine, and CNS conditions—ensuring regulatory compliance, protocol adherence, and participant safety. The role involves obtaining IRB approvals, managing the informed consent process, mentoring research staff, and serving as the primary point of contact with sponsors and regulators. This is an in-office position at up to 32 hours per week, offering a structured clinical research environment rather than traditional practice.
The company values professionalism and diversity in clinical research and prioritizes staff collaboration and development. You'll work under a medical director with three decades of investigator experience and access to established infrastructure across 20+ sites. Prior experience as a Principal or Sub-Investigator is preferred but not required; the essential qualifications are an active, unencumbered California MD or DO license and board certification or eligibility. The role demands strong organizational skills, familiarity with GCP guidelines and regulatory standards, and the ability to manage multiple projects in a fast-paced setting.
Compensation ranges from $130 to $150 per hour depending on experience and credentials. Full-time benefits include medical, dental, and vision coverage, HSA and FSA options, PTO, and disability and life insurance.
How this employer is doing
solid
- Expanding
- Recent Acquisition
In the news
Headlands Research Expands California Presence with Acquisition of Clinical Trials Research, PR Newswire
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Pay for this role
$130 to $150 per hour
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