Physician Principal Investigator
130–160 an hour
Behavioral Health Market Context
Apply Nowvia Marit Health
Job Description
ollaborative environment dedicated to diversity in clinical research.
Practice Info
• Two openings in the San Diego area: one at AMCR Institute in Escondido and one at Artemis Research near Serra Mesa
• AMCR Institute focuses on metabolic and immunologic research, including pre-diabetes, type 1 and type 2 diabetes, obesity, NAFLD/MASH, and vaccines
• Artemis Research specializes in psychiatry/neurology, internal medicine, and women's health studies
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
Compensation
• California Pay Range: $130-$160
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
• IV experience preferred, but not required
Practice Info
• Two openings in the San Diego area: one at AMCR Institute in Escondido and one at Artemis Research near Serra Mesa
• AMCR Institute focuses on metabolic and immunologic research, including pre-diabetes, type 1 and type 2 diabetes, obesity, NAFLD/MASH, and vaccines
• Artemis Research specializes in psychiatry/neurology, internal medicine, and women's health studies
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
Compensation
• California Pay Range: $130-$160
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
• IV experience preferred, but not required
Qualifications
- •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
Benefits
- •California Pay Range: $130-$160
Responsibilities
- •The successful candidates will contribute to advancing medical science within a supportive and collaborative environment dedicated to diversity in clinical research
- •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
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