Site Supervision Jobs in Eden Prairie, MN

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...

Buzz About Us: Welcome to Hunt Hive Talent Recruiting Agency where were all about connecting amazing talent with fantastic opportunities! Our mission To help businesses and professionals soar to new heights. If youre ready for an adventure in the world of site reliability engineering More...

Description: Full Stack Developer with the ability to work on production issues work in a war room trouble shoot and deploy code. Skills: 65% of work is as a Full Stack Engineer (Java backend with microservices / ReactJS front end) 35% of role is in an operational support leadersh More...

Description: Full Stack Developer with the ability to work on production issues work in a war room trouble shoot and deploy code. Skills: 65% of work is as a Full Stack Engineer (Java backend with microservices / ReactJS front end) 35% of role is in an operational support leadership More...

Description: Full Stack Developer with the ability to work on production issues work in a war room trouble shoot and deploy code. Skills: 65% of work is as a Full Stack Engineer (Java backend with microservices / ReactJS front end) 35% of role is in an operational support leade 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...

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...

Top Reasons to work with our client: Dynamic Industry: Be part of a leading mining operation with a focus on innovation! Career Development: Enjoy training and growth opportunities within the company! Competitive Compensation: Receive a strong salary and benefits package! Safety Co 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...

Under broad supervision analyzes the enterprise bus./tech. environment and participates in the operationalization of the enterprise data governance program (focus on policies standards procedures processes documentation and more). Job Summary: Under broad supervision analyzes the ent More...

Job Title: Manufacturing Production Supervisor Work location: Houston TX Job Type:C2C/Fulltime/W2 Job Description: At Alcon we are driven by the meaningful work we do to help people see brilliantly. We innovate ambitiously champion progress and act with speed as the global More...

Job Title: Manufacturing Production Supervisor Work location: Houston TX Job Type:C2C/Fulltime/W2 Job Description: At Alcon we are driven by the meaningful work we do to help people see brilliantly. We innovate ambitiously champion progress and act with speed as the global More...

Description: 12 months contract; TueWedThu (collaborative days) with flexibility to come in Mon and Fri as needed. Knowledge: Specific job responsibilities: Provides administrative support to supply chain teams for calendar management and travel arrangements. Manage new More...

Under broad supervision analyzes the enterprise bus./tech. environment and participates in the operationalization of the enterprise data governance program (focus on policies standards procedures processes documentation and more).Job Summary:Under broad supervision analyzes the enterp More...