Quality Investigator Jobs in Wooster, OH

Job Title: Quality Manager Location: Collinsville IL (Remote) Duration: 10 years Contract Must have: Deloittes Bridges Integrated Eligibility System (IES)/Illinois Integrated Eligibility System (IES) Responsible for reviewing and monitoring Vendor work for process quality deliver More...

Resource Management and Training:Participation in QM resource allocationResource allocation of QA auditorsFacilitation of professional development and career advancement of Quality Management staffAdministrative supervision of Quality Management staff jointly with Senior Director Qual More...

As Supplier Network Quality Engineer you will work and support Surface Treatment initiatives apply your knowledge of paint and surface treatment principals and work to certify suppliers to the company standard. You will provide supply chain expertise to buyers and suppliers while oper More...

Job Title: Quality Assurance Lead Location: Remote We are currently seeking candidates who meet the following qualifications: Responsibilities: Lead and mentor a team of QA engineers fostering a culture of quality and continuous improvement. Define and implement QA strategies methodo More...

About This Role The Senior Manager GCP Quality Assurance & Governance in R&D Quality and Compliance provides global strategic leadership for quality and oversight of quality activities in Biogen R&Ds ongoing clinical research and development processes and programs partneri More...

The Role The Data Quality & Integration Analyst will be responsible for ensuring data quality and integration for healthcare data supporting customers in valuebased care and collaborating with various teams. The role involves learning about population health performing data a More...

As Supplier Network Quality Engineer you will work and support Surface Treatment initiatives apply your knowledge of paint and surface treatment principals and work to certify suppliers to the company standard. You will provide supply chain expertise to buyers and suppliers while oper More...

Preferred locations include Denver CO Seattle WA Salt Lake City UT and Novato CA.  We are also willing to consider remote candidates. Applicants must be currently authorized to work in the United States on a fulltime basis. No sponsorship is available for this position.Are y More...

The Coder Quality Assurance Specialist will be accountable for executing the quality assurance program related to CODER services provided by Privia Health. The QA Specialist will serve as an integral member of the CODER program team responsible for partnering with vendor partners and 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...

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...

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: Must meet all requirements for Clinical Project Assistant position and have demonstrated proficiency in all relevant areas. Provides administrative assistance in site selection study implementation and ongoing coordination of study sites either directly or via CROs. Moni More...

Job Description: Job Title: Regulatory Studio Global Labeling Strategist (US 100% Remote)Work Location RemoteBill rate: BR5 BR/hrThe Global Labeling Strategist for Early Asset has overall accountability for initial creation and relevant updates to labeling documents (Target Label 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...

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...

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...

Drives key innovative and strategic projects and priorities for USMA oncology. Provides specialist medical/scientific strategic and operational input into core medical affairs activities such as: healthcare professional/provider interactions; generation of clinical and scientific data More...