Physician, MD/DO - Clinical Research

Headlands Research; Sacramento (CA); On-site; USD 216,000 - 250,000; Full time

Benefits offered by this job

Health insurance

HSA/FSA

PTO

Disability/Life insurance

EOE

Job summary

Headlands Research is hiring a Principal Investigator/ Sub-Investigator to lead and oversee clinical trials in our Sacramento sites, ensuring protocol adherence, regulatory compliance, and high-quality study execution.

The role requires CA licensure (MD/DO), board eligibility, and strong leadership. You will mentor staff, engage with sponsors, and promote diversity and inclusion across trials.

Qualifications

• Must hold an MD or DO license in California; board-certified or eligible.
• PI or Sub-Investigator experience preferred.
• Strong leadership and communication skills.
• Familiarity with GCP and regulatory guidelines.

Responsibilities

• Lead and oversee clinical trials, ensuring protocol and regulatory compliance.
• Mentor site staff, fostering inclusivity and professionalism within the team.
• Participate in investigator meetings and educational initiatives.
• Obtain IRB approval for study initiation and amendments.
• Oversee subject safety and informed consent processes.
• Communicate with sponsors, monitors, regulators, and leadership.
• Provide ongoing training and support to research staff.

Skills

Leadership

Regulatory compliance

GCP knowledge

Clinical oversight

Education

MD/DO with CA license

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.

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.

California Pay Range

$130 - $150 USD

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 [e-mail] 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.