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Headlands Research · 1 month ago

Part-time Physician - MD/DO

Escondido, California

Part-time

Onsite

Senior Level

$130/hr - $150/hr

Headlands Research is a leading network of advanced clinical trial sites dedicated to enhancing clinical trial delivery within communities. They are seeking a Board-Certified physician to serve as a Sub-Investigator at their AMCR site in Escondido, California, with responsibilities including assisting the Principal Investigator and ensuring compliance with clinical trial protocols.

BiotechnologyHealth CareMedical

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

Qualification

Board-Certified PhysicianVaccine ExperienceClinical Research ExperienceRegulatory Requirements KnowledgeClinical Practice (GCP)Communication SkillsLeadership SkillsOrganizational Skills

Required

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 have worked in vaccines. 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

Strong organizational skills and attention to detail, with the ability to manage multiple projects simultaneously in a fast-paced environment

Preferred

Previous experience as a Principal Investigator or Sub-Investigator for clinical research trials a huge plus, but willing to consider those without

Familiarity with regulatory requirements, Good Clinical Practice (GCP) guidelines, and industry best practices in clinical research or if inexperienced, a willingness to learn