Shipment Monitoring Jobs in South San Francisco, CA

We is seeking a Clinical Trial Specialist (CTS) or Senior CTS to assist in the execution of Clinical Trials. The successful candidate will be able to support the conduct of clinical trials with minimal guidance/supervision while ensuring alignment with GCP and Biogens SOPs. The S More...

We is seeking a Clinical Trial Specialist (CTS) or Senior CTS to assist in the execution of Clinical Trials. The successful candidate will be able to support the conduct of clinical trials with minimal guidance/supervision while ensuring alignment with GCP and Biogens SOPs. The S More...

We is seeking a Clinical Trial Specialist (CTS) or Senior CTS to assist in the execution of Clinical Trials. The successful candidate will be able to support the conduct of clinical trials with minimal guidance/supervision while ensuring alignment with GCP and Biogens SOPs. The S More...

We is seeking a Clinical Trial Specialist (CTS) or Senior CTS to assist in the execution of Clinical Trials. The successful candidate will be able to support the conduct of clinical trials with minimal guidance/supervision while ensuring alignment with GCP and Biogens SOPs. The S More...

We is seeking a Clinical Trial Specialist (CTS) or Senior CTS to assist in the execution of Clinical Trials. The successful candidate will be able to support the conduct of clinical trials with minimal guidance/supervision while ensuring alignment with GCP and Biogens SOPs. The S More...

We is seeking a Clinical Trial Specialist (CTS) or Senior CTS to assist in the execution of Clinical Trials. The successful candidate will be able to support the conduct of clinical trials with minimal guidance/supervision while ensuring alignment with GCP and Biogens SOPs. The S More...

We is seeking a Clinical Trial Specialist (CTS) or Senior CTS to assist in the execution of Clinical Trials. The successful candidate will be able to support the conduct of clinical trials with minimal guidance/supervision while ensuring alignment with GCP and Biogens SOPs. The S 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...

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...

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...

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 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...

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...

Job Title: Quality Manager Location: Collinsville IL (Remote) Duration: 10 years Contract Must have: Deloittes Bridges Integrated Eligibility System (IES)/Illinois Integrated Eligibility System (IES) Responsible for reviewing and monitoring Vendor work for process quality deliver More...

Title: NOC/SOC Engineer Location: Remote Job Description Operations Run the NOC L1 & L2 activities Responsible for the operations monitoring and management of the Splunk infrastructure and services Investigate diagnose and remediate NOC incidents Manage NOC incidents lifecy More...

Maintain responsibility for the design deployment and maintenance of productionscale systems. Support services before they go live using activities including system designing consulting developing software platforms and frameworks capacity planning and launching reviews. Measure monit More...

Maintain responsibility for the design deployment and maintenance of productionscale systems. Support services before they go live using activities including system designing consulting developing software platforms and frameworks capacity planning and launching reviews. Measure monit More...

Maintain responsibility for the design deployment and maintenance of productionscale systems. Support services before they go live using activities including system designing consulting developing software platforms and frameworks capacity planning and launching reviews. Measure monit More...