Cctv Monitoring Jobs in Virginia Beach, VA

AECOM is seeking Traffic Monitoring Operator(s) located in Virginia Beach VA. The shift hours available for the position(s) are 1st shift (5:15 am to 1:45 pm) 2nd shift (1:15pm 9:45 pm) and/or 3rd shift (9:15 pm 5:45 am). Shift will be assigned after training is completed. More...

AECOM is seeking Traffic Monitoring Operator(s) located in Virginia Beach VA. The shift hours available for the position(s) are 1st shift (5:15 am to 1:45 pm) 2nd shift (1:15pm 9:45 pm) and/or 3rd shift (9:15 pm 5:45 am). Shift will be assigned after training is completed. More...

AECOM is seeking Traffic Monitoring Operator(s) located in Virginia Beach VA. The shift hours available for the position(s) are 1st shift (5:15 am to 1:45 pm) 2nd shift (1:15pm 9:45 pm) and/or 3rd shift (9:15 pm 5:45 am). Shift will be assigned after training is completed. More...

AECOM is seeking Traffic Monitoring Operator(s) located in Virginia Beach VA. The shift hours available for the position(s) are 1st shift (5:15 am to 1:45 pm) 2nd shift (1:15pm 9:45 pm) and/or 3rd shift (9:15 pm 5:45 am). Shift will be assigned after training is completed. More...

AECOM is seeking Traffic Monitoring Operator(s) located in Virginia Beach VA. The shift hours available for the position(s) are 1st shift (5:15 am to 1:45 pm) 2nd shift (1:15pm 9:45 pm) and/or 3rd shift (9:15 pm 5:45 am). Shift will be assigned after training is completed. More...

AECOM is seeking Traffic Monitoring Operator(s) located in Virginia Beach VA. The shift hours available for the position(s) are 1st shift (5:15 am to 1:45 pm) 2nd shift (1:15pm 9:45 pm) and/or 3rd shift (9:15 pm 5:45 am). Shift will be assigned after training is completed. 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 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...

Job Title Validation Process Monitoring and Data Analytics Engineer Location Parsippany NJ Hybrid Onsite T/W/Th Working hours: 84:30 8:305 95:30 type of hours (most of team works 95) Job Duration: 12 months Responsibilities: Strong background in statistics process monitori 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...

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...

PSI Medical Monitors provide medical input to global clinical studies and advise the teams and business partners while always focusing on patients safety and wellbeing.HomeBased in the United StatesResponsibilities:Advise clients project teams sites data safety monitoring boards More...

Job Responsibilities:Consult with customers business users and technology specialists to identify and document business processes and data flows identify and document detailed business requirements related to the business processes document gap analysis and assist with the development More...

The Vendor Performance Manager Medical Coding and Billing leads the vendor management team in implementing and managing a formalized process for selecting monitoring and auditing thirdparty medical coding and billing vendors. This includes overseeing all aspects of the vendor managem More...