Principal Investigator - Psychiatry/Neurology

Kinetic Clinical Research • West Covina, CA

21d • $150 - $300

About The Position

Kinetic Clinical Research is seeking a board-certified physician to lead clinical trials in psychiatry and neurology across its Southern California locations. The Principal Investigator will design and implement research protocols, oversee studies from participant recruitment through completion and follow-up, provide clinical oversight, and ensure participant safety, data integrity, and regulatory compliance. The role includes supervising and mentoring research staff, collaborating with multidisciplinary teams, training staff on protocols, and representing the organization during inspections and audits. Spanish proficiency is preferred to support the region’s diverse patient population.

Requirements

• MD or DO degree and completed residency in Psychiatry, Neurology, or a related specialty.
• Board certification in Psychiatry or Neurology.
• Current California medical license.
• Active DEA registration.
• Deep expertise in psychiatric and neurological disorders.
• Proven experience with regulatory submissions and agency interactions.
• Strong clinical research methodology background.
• Exceptional clinical judgment and decision-making skills.
• Outstanding written and verbal communication abilities.
• Proficiency with research databases and electronic data capture systems.
• Ability to independently manage multiple complex projects.

Nice To Haves

• Fellowship training in a relevant subspecialty.
• Experience with CNS therapeutics and biomarker research.
• Track record of peer-reviewed publications.
• Spanish proficiency in reading, writing, and speaking.

Responsibilities

• Serve as Principal Investigator on multiple clinical trials in psychiatry and neurology.
• Design and implement research protocols in compliance with FDA, ICH-GCP, and institutional guidelines.
• Oversee all study phases, from patient recruitment through completion and follow-up.
• Ensure data integrity and quality across clinical trials.
• Conduct clinical assessments and evaluations of study participants.
• Make medical decisions concerning participant safety and study continuation.
• Supervise research coordinators and clinical study staff.
• Maintain medical records and research documentation.
• Maintain adherence to Good Clinical Practice standards and stay current with regulatory requirements and industry practices.
• Represent the organization during regulatory inspections and audits.
• Submit timely, accurate reports to sponsors, IRB/Ethics Committees, and regulatory bodies.
• Mentor and develop research staff, including coordinators, nurses, and data managers.
• Collaborate with multidisciplinary teams, including statisticians and sponsors.
• Deliver training on study protocols and procedures.

Benefits

• Competitive compensation.
• Flexible schedule and hours.
• Professional growth through work with cutting-edge research and diverse patient populations.
• Collaborative work environment.

What This Job Offers

• Job Type: Part-time
• Career Level: Principal
• Education Level: Ph.D. or professional degree