Site Environment Jobs in King of Prussia, PA

In this role a Site Technology Specialist: Provides clinical sites with technical support and expertise related to technology.Assists in the design and implementation of study related forms guidelines and manuals related to technologiesCoordinates data collection related to techn More...

The Site Contract Specialist can be based anywhere in the United States. The core responsibilities of this role include:Facilitating negotiations of site agreements and budgets to ensure alignment with the site activation plan Customizing and preparing country More...

The Site Contract Specialist can be based anywhere in the United States. The core responsibilities of this role include:Facilitating negotiations of site agreements and budgets to ensure alignment with the site activation plan Customizing and preparing country More...

Hybrid role in King of Prussia PASite ManagementEnsures exchange of information and documentation with sites and vendorsEnsures order receipt inventory storage distribution return/recall and reconciliation of clinical suppliesEnsures regulatory and ethics committee submissions and not More...

The Site Contract Specialist can be based anywhere in the United States. The core responsibilities of this role include:Facilitating negotiations of site agreements and budgets to ensure alignment with the site activation plan Customizing and preparing country More...

Hybrid role in King of Prussia PASite ManagementEnsures exchange of information and documentation with sites and vendorsEnsures order receipt inventory storage distribution return/recall and reconciliation of clinical suppliesEnsures regulatory and ethics committee submissions and not More...

This role requires a US Citizen or Green Card holder. Your CareerThe Cortex team builds and delivers the industrys most advanced SecOps platform consisting of XSIAM XSOAR and XPANSE. As a member of the Cortex DevOps team  your role involves operating and maintaining a larges 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...

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...

We are seeking a dynamic and motivated Business Development Representative to join our team. This individual will be responsible for identifying engaging and recruiting physicians to join our Clinical Trial Site Enablement Organization (SEO). The ideal candidate will have a stron More...

Description: Title: Environment Health and Safety Specialist II Shift: MoFr 7am 4pm (estimated start/end) Knowledge of building construction and demolition safety and environmental practices Knowledge of current national and state safety and environmental legislation Knowledge 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...

Acts as a specialized liaison to assist sites with a protocoltailored approach to increase efficiency of the patient identification and recruitment processAssists sites in developing and implementing patient enrollment techniquesCoordinates site specific patient recruitment and retent More...

We are seeking an experienced Clinical Research Billing Specialist to join our Site Enabling Organization (SEO). This role is critical for ensuring accurate and compliant billing of clinical research activities from the site side with particular attention to differentiating between re More...

Solution IT Inc. is looking for a Oracle Cloud Demand Planning Functional for one of its clients in Southern CA / Occasional Travel Mostly remote but some client trips to Southern CA Expenses Paid Job Title: Oracle Cloud Demand Planning Functional Required Skills: 10 years progressiv More...

The official title for this role will be Regional Project Lead.The Regional Project Lead manages and coordinates activities of project teams in designated countries and ensures consistency of Clinical Operations processes across regions. They ensure meeting study milestones are met by More...