Fda Regulations Jobs in San Diego, CA

For further inquiries regarding the following opportunity please contact our Talent Specialist: Meghna at Title: Systems Engineer 3 Location: San Diego CA Duration: 5 months Job Description : Must Haves: 1. Configuration Management Expertise: Proven understanding and More...

For further inquiries regarding the following opportunity please contact our Talent Specialist: Meghna at Title: Systems Engineer 3 Location: San Diego CA Duration: 5 months Job Description : Must Haves: 1. Configuration Management Expertise: Proven understanding and More...

As a Clinical Research Physician you will provide clinical mentorship and leadership for clinical development and clinical trials conduct within our organization. You will operate in a wide range of aspects in clinical and pharmaceutical medicine and with patients health authorities c More...

For further inquiries regarding the following opportunity please contact our Talent Specialist: Infant at Title: R&D Portfolio Manager Location: San Diego CA Duration: 9 Months (with possible extension) Remote Workplace: Your location will be a home office; you are not require More...

SummaryThe Clinical Operations Director is responsible for overseeing the tactical implementation of the clinical development plan for autoimmune studies. This includes managing timelines budgets resources and clinical staff to ensure efficient and highquality execution of clinical tr 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...

Resource Management and Training:Participation in QM resource allocationResource allocation of QA auditorsFacilitation of professional development and career advancement of Quality Management staffAdministrative supervision of Quality Management staff jointly with Senior Director Qual More...

Resource Management and Training:Participation in QM resource allocationResource allocation of QA auditorsFacilitation of professional development and career advancement of Quality Management staffAdministrative supervision of Quality Management staff jointly with Senior Director Qual More...

The Quality Assurance Specialist will be responsible for routinely reviewing analysis reports to ensure their accuracy completeness and compliance with internal/external guidelines.  As part of this review candidates will identify/initiate CAPAs Deviations Change Controls Process More...

Resource Management and Training:Participation in QM resource allocationResource allocation of QA auditorsFacilitation of professional development and career advancement of Quality Management staffAdministrative supervision of Quality Management staff jointly with Senior Director Qual 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...

Resource Management and Training:Participation in QM resource allocationResource allocation of QA auditorsFacilitation of professional development and career advancement of Quality Management staffAdministrative supervision of Quality Management staff jointly with Senior Director Qual More...

Resource Management and Training:Participation in QM resource allocationResource allocation of QA auditorsFacilitation of professional development and career advancement of Quality Management staffAdministrative supervision of Quality Management staff jointly with Senior Director Qual More...

Resource Management and Training:Participation in QM resource allocationResource allocation of QA auditorsFacilitation of professional development and career advancement of Quality Management staffAdministrative supervision of Quality Management staff jointly with Senior Director Qual More...