Plan Review Jobs in Lancaster, NE

This role presents an extraordinary opportunity for a missiondriven leader to play an integral role in supporting the finance and health plan operations of a dynamic integrated care delivery program. Responsible for managing and continuously improving our LIFE/PACE Health Plan Operati More...

This role presents an extraordinary opportunity for a missiondriven leader to play an integral role in supporting the finance and health plan operations of a dynamic integrated care delivery program. Responsible for managing and continuously improving our LIFE/PACE Health Plan Operati More...

This role is not a coding or data science role. We are not currently seeking computer science or ITbackground applicants for these roles.Ensure that the client receives quality data by reviewing laboratory data for accuracy clarity and adherence to GMP and/or GLP regulationsReview sim More...

This role is not a coding or data science role. We are not currently seeking computer science or ITbackground applicants for these roles.Ensure that the client receives quality data by reviewing laboratory data for accuracy clarity and adherence to GMP and/or GLP regulationsReview sim More...

This role is not a coding or data science role. We are not currently seeking computer science or ITbackground applicants for these roles.Ensure that the client receives quality data by reviewing laboratory data for accuracy clarity and adherence to GMP and/or GLP regulationsReview sim More...

This role is not a coding or data science role. We are not currently seeking computer science or ITbackground applicants for these roles.Ensure that the client receives quality data by reviewing laboratory data for accuracy clarity and adherence to GMP and/or GLP regulationsReview sim More...

Job Summary: Eurofins Microbiology is seeking an Associate Scientist to support data quality by reviewing laboratory data for accuracy precision and adherence to GMP and/or GLP regulations. This position does not require previous experience in the pharmaceutical industry and prov More...

This role is not a coding or data science role. We are not currently seeking computer science or ITbackground applicants for these roles.Ensure that the client receives quality data by reviewing laboratory data for accuracy clarity and adherence to GMP and/or GLP regulationsReview sim More...

Eurofins Biopharmaceutical is looking for an Associate Scientist to support Data Review of our Biochemistry team. The Associate Scientist position is considered an entrylevel opportunity that will allow for hands on development and growth in daytoday acti More...

Eurofins Biopharmaceutical is looking for an Associate Scientist to support Data Review of our Biochemistry team. The Associate Scientist position is considered an entrylevel opportunity that will allow for hands on development and growth in daytoday acti More...

This role is not a coding or data science role. We are not currently seeking computer science or ITbackground applicants for these roles.Ensure that the client receives quality data by reviewing laboratory data for accuracy clarity and adherence to GMP and/or GLP regulationsReview sim 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...

Description: Job Title: Clinical Trials Management Associate II Location: Foster City CA Duration: 06 months with possible extension Shift Details: 1st shift/ Monday Friday 8am5pm/business hours Essential Duties and Responsibilities Leads or manage components of Phase I II 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...

The Lead Data Manager is responsible for all data management activities in assigned clinical trials under supervision.Acts as primary communication point for project teams and company departments regarding clinical data managementActs as primary communication point for clients/vendors More...

Top reasons to work for our client: Great team environment! Manager is well respected by team! Inclusive Workplace Awesome career development opportunities! Competitive Rates Job Type : Full Time Location : Westwood Massachusetts Pay : Great Pay Benefits! Job Descripti 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 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...