Sub-Investigator Physician
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Job Description
About Company
The job is for a position at the Artemis Institute of Clinical Research site, located in Riverside, California, which is part of Headlands Research. Headlands Research is dedicated to building a diverse and talented team, including clinical research coordinators, research assistants, physicians, advanced providers, and patient recruitment specialists. They emphasize ample support, a culture of collaboration, and a high level of professionalism as key differentiators within their organization.
Job Description
This is a job posting for an Internal Medicine/Emergency Medicine/Family Practice physician to serve as a Sub-Investigator.
• Role Title: Sub-Investigator
• Specialties Considered: Internal Medicine, Emergency Medicine, Family Practice, Urgent Care, Endocrinology, Rheumatology, and other relevant specialties.
• Employment Type: Part-time Employee
• Location: Onsite in Riverside, California (Artemis Institute of Clinical Research site). No opportunities for remote or hybrid work.
• Schedule: Ideally three days per week (Mondays through Wednesdays) for 8-hour shifts, totaling approximately 24 hours/week. Clinic hours are from 7:00 am – 3:30 pm. The company is flexible and willing to discuss other scheduling options.
• Pay: Competitive, ranging from $130-150/hour, dependent upon years of experience as an Investigator in clinical research.
Why Join (Benefits & Work Environment):
• Offers a flexible schedule to fit personal life.
• Provides a dynamic team environment with ample support.
• Fosters a culture of collaboration, where individual contributions are valued and make a difference.
• Emphasizes a high level of professionalism.
Responsibilities:
• Assist the Principal Investigator in conducting clinical trials at Headlands Research sites.
• Ensure full compliance with protocol requirements, regulatory standards, and ethical guidelines.
• Provide leadership and mentorship to site staff, promoting a culture of inclusivity, diversity, and professionalism.
• Participate in investigator meetings and educational initiatives to stay current with advancements in clinical research and diversity initiatives.
• Obtain Institutional Review Board (IRB) approval for study initiation and any protocol modifications.
• Oversee subject safety, ensure compliance with trial conduct, and manage the informed consent process.
• Communicate effectively with various 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 is a significant advantage, but candidates without prior experience will also be considered.
• Must be eligible for or hold an active, unencumbered license to practice as an MD or DO within the state of California.
• Must be board-certified or board-eligible in a relevant specialty.
• Possess excellent communication and leadership skills, with the ability to effectively collaborate with sponsors, research teams, and external stakeholders.
• Familiarity with regulatory requirements, Good Clinical Practice (GCP) guidelines, and industry best practices in clinical research is preferred, but a willingness to learn is acceptable for those without prior experience.
• Demonstrate strong organizational skills and attention to detail, capable of managing multiple projects simultaneously in a fast-paced environment.
