Clinical Research Jobs in San Diego, CA

As a Clinical Research Associate at PSI you will enjoy a variety of monitoring tasks and work on clinical studies in different therapeutic indications maintaining the highest quality standards in the industry.You will:Act as the main line of communication between the project team spon More...

Description: The ideal candidate will have thorough knowledge of Clinical investigation of medical devices for human subjects Good Clinical Practice (ISO 14155) 21 CFR partand other applicable regulations. Roles & Responsibilities: Contribute to all clinical research activitie More...

As a Clinical Research Associate at PSI you will enjoy a variety of monitoring tasks and work on clinical studies in different therapeutic indications maintaining the highest quality standards in the industry.You will:Act as the main line of communication between the project team spon More...

As a Senior CRA you will work on the frontline of communication with project stakeholders ensuring timelines targets and standards of clinical research projects in a variety of therapeutic indications.  You will build and maintain relationships with clinical sites and investigato More...

As a Clinical Research Associate at PSI you will enjoy a variety of monitoring tasks and work on clinical studies in different therapeutic indications maintaining the highest quality standards in the industry.You will:Act as the main line of communication between the project team spon More...

As a Clinical Research Associate at PSI you will enjoy a variety of monitoring tasks and work on clinical studies in different therapeutic indications maintaining the highest quality standards in the industry.You will:Act as the main line of communication between the project team spon More...

Coordinates investigator/ site feasibility and identification process as well as study startup.Monitors project timelines and patient enrollment implements respective corrective and preventive measures.Reviews monitoring visit reports for all visit types and ensures reporting complian More...

The SubInvestigator provides oversight in medical and clinical issues as requested or required. The SubInvestigator works with the Principal Investigator (PI) to evaluate clinical trials and ensure that all studyrelated procedures are completed in accordance with Good Clinical Practic More...

The SubInvestigator provides oversight in medical and clinical issues as requested or required. The SubInvestigator works with the Principal Investigator (PI) to evaluate clinical trials and ensure that all studyrelated procedures are completed in accordance with Good Clinical Practic More...

The SubInvestigator provides oversight in medical and clinical issues as requested or required. The SubInvestigator works with the Principal Investigator (PI) to evaluate clinical trials and ensure that all studyrelated procedures are completed in accordance with Good Clinical Practic More...

The SubInvestigator provides oversight in medical and clinical issues as requested or required. The SubInvestigator works with the Principal Investigator (PI) to evaluate clinical trials and ensure that all studyrelated procedures are completed in accordance with Good Clinical Practic More...

The SubInvestigator provides oversight in medical and clinical issues as requested or required. The SubInvestigator works with the Principal Investigator (PI) to evaluate clinical trials and ensure that all studyrelated procedures are completed in accordance with Good Clinical Practic More...

The SubInvestigator provides oversight in medical and clinical issues as requested or required. The SubInvestigator works with the Principal Investigator (PI) to evaluate clinical trials and ensure that all studyrelated procedures are completed in accordance with Good Clinical Practic More...

The SubInvestigator provides oversight in medical and clinical issues as requested or required. The SubInvestigator works with the Principal Investigator (PI) to evaluate clinical trials and ensure that all studyrelated procedures are completed in accordance with Good Clinical Practic More...

Summary:The Clinical Trial Manager (CTM) is responsible for managing and supporting clinical trials in compliance with applicable regulations ICH/GCP guidelines and standard operating procedures (SOPs). The CTM works collaboratively with crossfunctional teams and partners with interna More...

Description: Job Title: Research Associate III/ Histology Technical Specialist Location: Foster City CA Duration: 11 months with possible extension Shift Details: 1st shift/ Monday Friday 8am5pm/business hours Pay Range: Negotiable Essential Duties and Responsibilities O More...

This Position is Contingent Upon Contract Award.This position is in support of a proposed repatriation initiative.  The purpose of the facilities is to provide comprehensive care for migrant individuals who are awaiting reunification or repatriation. This care will begin as soon More...

This Position is Contingent Upon Contract Award.This position is in support of a proposed repatriation initiative.  The purpose of the facilities is to provide comprehensive care for migrant individuals who are awaiting reunification or repatriation. This care will begin as soon More...

Industry: HealthcareClinical Nurse Specialist CVICULocation: Santa Clara CAResponsibilities:Clinical Expertise: Provide expert consultation and guidance to nurses and other healthcare providers in the CVICU.Education & Mentorship: Develop and implement educational programs for nu More...

Job Title Research Associate III Histology Technical Specialist Location Foster City CA 94404 Duration 12 months Job Summary: The Pathobiology Lab Operations Group is seeing an experienced Histology Technician to enhance our pathology and translational research efforts. Th More...