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Internal Medicine MD/DO - Clinical Research - Better Work/Life Balance
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Internist Job at Headlands Research in Riverside, CA
Physician | Internal Medicine Job | Riverside, CA 92503-4955
Internal Medicine MD/DO - Clinical Research - Better Work/Life Balance
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Physician-Internal Medicine
Employment Type: Part-Time
Telemedicine : No 
Practice Type: Group Practice
Salary Range: NegotiableJob Description
The Role of a Lifetime
Are you ready to make a difference? We're seeking an Internal Medicine/Emergency Medicine/Family Practice physician to serve as a Sub-Investigator to help us grow our Artemis Institute of Clinical Research site located in Riverside, California. Ideally, we are seeking someone for three days per week (M, T, W) for 8-hours each day. However, we are flexible in our needs and we want to speak with you if you have other thoughts in mind.
Why Join Us?
- Flexible Schedule: Work on your terms, with a schedule that fits your life.
- 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.
Type: Part-time Employee (~24 hours/week, but willing to discuss other options!)
Pay: Competitive and dependent upon years of experience as an Investigator in clinical research. Range is $130-150/hour.
Location: Onsite in Riverside, California (no opportunities for remote or hybrid)
Schedule: Mondays through Wednesdays, 8-hour shifts (clinic hours are from 7:00am-3:30pm)
Responsibilities:
- Assist the Principal Investigator with conducting clinical trials 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(when necessary 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 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 California required
- Must be board-certified or board-eligible and we are open to a variety of specialties (Internal Med/Emergency Med/Urgent Care/Family Practice/Endocrinology/Rheumatology...).
- 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 or if inexperienced, a willingness to learn.
- Strong organizational skills and attention to detail, with the ability to manage multiple projects simultaneously in a fast-paced environment.
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