Jobs at Irvine Clinical Research

Coordinate Phase II/III clinical trials onsite: manage study operations, ensure GCP/FDA protocol compliance, enroll and coordinate participants, perform clinical assessments (vitals, ECGs), enter and maintain eSource/EDC/CTMS data, and maintain regulatory readiness for monitoring and audits.

Provide clinical oversight as a Sub-Investigator for Alzheimer’s disease trials: screen participants, manage safety and adverse events, perform exams, infusions, phlebotomy, and coordinate with physicians and study coordinators to ensure protocol compliance and participant care.

The clinician will oversee clinical trials for Alzheimer's Disease treatments, manage safety, conduct eligibility interviews, and perform assessments.

The Clinical Scientist will prescreen and screen candidates for clinical trials, assess participants using clinical judgment, and communicate trial details effectively.

The Neurologist Principal Investigator will lead clinical trials in memory disorders, manage trial safety, educate participants, and oversee a study team.

The Clinical Research Recruitment Coordinator recruits study participants through phone interviews, promotes services, and manages data input and outreach efforts.