Site Surveys Jobs in Grand Prairie, TX

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...

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...

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...

Position: Data Entry Clerk Work From Home PartTime Focus Group Participants (Side Gig)We are seeking individuals to participate in National & Local Paid Focus Groups Clinical Trials Phone Interviews or Paid Surveys.With most of our paid surveys you have the option to participate remo More...

Position: Data Entry Clerk Work From Home PartTime Focus Group Participants (Side Gig)We are seeking individuals to participate in National & Local Paid Focus Groups Clinical Trials Phone Interviews or Paid Surveys.With most of our paid surveys you have the option to participate remo More...

Engagement Type Contract Short Description ABC Senior BSA ON SITE REQUIRED: 3 days/week (NO Exceptions). Parking IS provided on site for contractors Complete Description 3 days/week ON SITE required from Day 1. No Exceptions! Pls make sure they understand they will be required to 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...

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...

NCDHHS seeks a Expert Business Analyst tosupport the business case development process improvement and requirementsanalysis testing and implementation project for new software solution for NCChild Support Services. Child Support experience required.Primary tasks include: Identify a More...

Your CareerThe Supply Chain Compliance Manager will drive compliance  programs within the supply chain focusing on ensuring our products meet regulatory requirements.  This role includes staying current with global regulations conducting gap assessments and ensuring complian More...

Follow SOP and Work Instructions update as needed and ensure financial closing requirements as well as forecasting and closing all books timelyEnsure all vendor invoices & monthly customer invoice is submitted & paid timelyCheck with vendors for new invoices keeping track of w 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...

General SummaryUnder the supervision of the Director of Payer Relations & Contracting serves as key liaison to UMMC and FPI leadership as well as physician clinical and administrative staff for physician and hospital specialized highcost service contracting.  Acting as the pr More...