Jobs at Irvine Clinical Research

Manage daily operations of clinical trials, perform study procedures per GCP and protocols, maintain paper and electronic study data, engage patients and sponsors, work with recruitment to meet enrollment goals, and conduct diagnostic, efficacy, and safety assessments.

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 Research Nurse will administer investigational drugs, monitor participant safety, perform medical procedures, and ensure accurate study data collection.

The Clinical Research Financial Analyst manages financial processes for clinical trials, ensuring billing accuracy and revenue capture through collaboration and detailed financial reporting.

The Clinical Research Coordinator I will manage day-to-day operations of clinical trials, including participant recruitment and data management under supervision.

As a Research Dietitian/Coordinator, you'll counsel study participants on nutrition and lifestyle, manage clinical trial operations, and ensure compliance with protocols.

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

The Sub-Investigator will manage clinical trials for Alzheimer's Disease, overseeing the safety of participants and conducting evaluations and intake interviews.

The Clinical Scientist/Neuropsychological Rater will assess study participants, conduct interviews, inform about clinical trials, and assist with study operations.

The Clinical Research Coordinator manages clinical trial operations, ensures compliance with protocols, and works on patient recruitment and assessment, with a focus on Alzheimer's research.

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 Site Manager oversees site operations, manages teams, drives financial and enrollment goals, and ensures compliance in clinical studies.

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

The Research Assistant will provide administrative support to physicians and researchers, assist with data entry, manage scheduling, and greet participants, particularly older adults.