Manager Associate Regulatory Trials Clinical Mwd Jobs in Modesto, CA

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 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...

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: Clinical Data Associate Duration: 06 months contract with possible extension Shift Details: Day shift/ Fully Remote Pay Range: $30$37 /hr w2 Essential Duties and Responsibilities: Works collaboratively with Process Engineers and Statisticians in Global Manufact 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 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...

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...

insightsoftware is hiring an experienced Regulatory & Export Compliance Manager to support the business develop continuously enhance scale and manage insightsoftwares regulatory and export compliance including matters pertaining to antibribery/anticorruption and ethics. A successf More...

Vice President Regulatory AffairsHybrid/Remote Options AvailableAre you a strategic leader with a passion for regulatory compliance and higher education Join our team as Vice President of Regulatory Affairs where you will shape compliance strategies build key regulatory relationships More...

At Adtalem Global Education we are committed to empowering students and transforming lives through education. As a Senior Regulatory Affairs Analyst you will play a critical role in ensuring compliance with federal state and accreditor regulations helping to shape policies and process More...

Overview: TekWissen is a global workforce management provider headquartered in Ann Arbor Michigan that offers strategic talent solutions to our clients worldwide. The below job opportunity is with one of our Biotech clients who researches develop and commercializes drugs. The com More...

Your CareerThe Global Regulatory and ESG Compliance Manager will drive ESG programs within the supply chain focusing on human rights environmental standards and sustainable practices. This role includes staying current with global regulations conducting gap assessments and ensuring co More...

Your CareerThe Global Regulatory and ESG Compliance Manager will drive ESG programs within the supply chain focusing on human rights environmental standards and sustainable practices. This role includes staying current with global regulations conducting gap assessments and ensuring co More...

Your CareerThe Global Regulatory and ESG Compliance Manager will drive ESG programs within the supply chain focusing on human rights environmental standards and sustainable practices. This role includes staying current with global regulations conducting gap assessments and ensuring co More...

Your CareerThe Global Regulatory and ESG Compliance Manager will drive ESG programs within the supply chain focusing on human rights environmental standards and sustainable practices. This role includes staying current with global regulations conducting gap assessments and ensuring co More...

Your CareerThe Global Regulatory and ESG Compliance Manager will drive ESG programs within the supply chain focusing on human rights environmental standards and sustainable practices. This role includes staying current with global regulations conducting gap assessments and ensuring co More...