Principal Investigator (Psychiatry)

About the role

This is a 1099 Independent Contractor position. The Principal Investigator (PI) is responsible for conducting objective clinical research, managing and overseeing the research project, and coordinating with necessary departments to ensure compliance with federal regulations and sponsoring agency policy and procedures.

Responsibilities

• Manage and monitor the design, conduct, and reporting of the research project
• Direct and oversee compliance, financial, personnel, and other related aspects of the research project
• Collaborate with necessary departments to ensure research is conducted in accordance with federal regulations and sponsoring agency policy and procedures
• Minimize risks to research subjects by using procedures consistent with sound research design and avoiding unnecessary exposure to risk
• Inform human research subjects of risks and benefits of research participation, obtain informed consent, and maintain confidentiality of data
• Monitor data collection to ensure safety of human research subjects
• Respond promptly to requests for information, submit research studies for renewal, and ensure adequate resources and facilities are available
• Inform associates, colleagues, and personnel of study procedures, informed consent requirements, potential adverse events, reportable new information, and data collection and record-keeping criteria
• Conduct the study in strict accordance with the approved research protocol, document informed consent in accordance with approved informed consent documents, and maintain accurate research subject records
• Report promptly any internal or external adverse events, significant changes in the risk/benefit of study participation, and ensure adequate care is provided to research subjects experiencing significant adverse events
• Keep human research subjects fully informed of any new information affecting their willingness to continue participating in the research study
• Ensure all listed investigators have appropriate credentials and complete required training modules
• Adhere to Good Clinical Practice guidelines and ensure conduct of the research study adheres to these guidelines
• Work in close collaboration with company quality and clinical operational oversight

Qualifications

• A valid medical degree (MD or DO)
• 5+ years of clinical research experience as a PI or Sub-Investigator
• Proficient with Microsoft Office Suite
• An active medical license in good standing, with unrestricted ability to practice in place of work, where applicable
• Demonstrated leadership skills, including strong communication, presentation, written, and interpersonal skills
• Results-driven, with a track record of building, managing, and motivating teams to meet or exceed clinical goals and objectives
• Strong analytical and decision-making capabilities that support clinical continuous improvement initiatives
• Advanced organizational and project management abilities, including the ability to work within tight deadlines on a range of projects
• Self-starter and highly motivated individual who can identify needs and proactively work to solve problems and gaps

Benefits

• Medical
• Dental
• Vision
• 401(k)
• Company Paid Short Term Disability
• Flexible Spending Account (FSA)
• Health Savings Account (HSA)
• Paid Time Off
• Voluntary Benefits

Pay

The typical base pay range for this role is USD $156,600 - $266,700 per year. Individual base pay depends on various factors, in addition to primary work location, complexity and responsibility of role, job duties/requirements, and relevant experience, skills, and other market-based factors.

Schedule

N/A