M3 Wake Research is a leading independent clinical research network with nearly 30 owned and managed sites nationwide. Conducting studies since 1984, Wake Research has completed more than 7,000 clinical trials and maintains a proprietary U.S. patient database. The organization is known for high-quality execution, regulatory compliance, timely enrollment, and reliable data delivery.
Position: APP Sub-Investigator / Clinical Trial Rater
M3 Wake Research is seeking a full-time, onsite APP Sub-Investigator/Rater to support clinical trials at its Mission Viejo and Encino, CA sites.
Role Overview
The Sub-Investigator works closely with the Principal Investigator to conduct clinical trials in compliance with GCP, FDA, and ICH standards. Responsibilities include participant evaluations, informed consent support, protocol-driven visits, rater scale administration, documentation, and safeguarding participant health and safety. This role may also support study coordination as needed.
Key Responsibilities
Qualifications
Compensation & Benefits
M3 Wake Research, Inc., one of the largest independent clinical research site services companies in North America with more than 18 owned and managed research sites across seven states in the US and continues to grow.
This site is only intended for job seekers to contact the organizations posting jobs. Use of this site for solicitation and other unintended purposes is prohibited. Job ads are supplied by the employer. PracticeMatch does not verify postings and is not responsible for legal compliance. Employers are solely responsible for complying with all applicable job-posting and pay-transparency requirements.