Quality Engineer II
Talent Software Services
Mason, OH
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JOB DETAILS
SALARY
$50–$60 Per Hour
JOB TYPE
Full-time, Employee
SKILLS
Analysis Skills, Communication Skills, Control Systems, Document Control, Electricity, Electromechanics, Failure Analysis, Laboratory, Manufacturing, Mechanical Engineering, Medical Equipment, Mentoring, Microsoft Excel, Microsoft Office, Microsoft Outlook, Microsoft PowerPoint, Microsoft Word, Multitasking, Operations Management, Performance Analysis, Power BI, Presentation/Verbal Skills, Problem Solving Skills, Product Support, Quality Assurance Methodology, Quality Engineering, Research & Development (R&D), Root Cause Analysis, SAP, Standard Operating Procedures (SOP), Systems Analysis, Team Player, Test Plan/Schedule, Training/Teaching, Vendor/Supplier Management, Writing Skills
LOCATION
Mason, OH
POSTED
21 days ago
Clinical Trial Manager
Job Summary: Talent Software Services is in search of a Clinical Trial Manager for a contract position in Mason, OH. The opportunity will be for 12 months with a strong chance for a long-term extension.
Primary Responsibilities/Accountabilities:
- Procedural work and expertise in Application work by combining hands-on experimentation with scientific principles and knowledge from science/engineering education to drive foundational technical understanding and solve technical problems. Delivers technical outputs that address critical innovation challenges and the completion of key milestones.
- The Clinical Trial Manager (CTM) is a key member of the clinical team with responsibility for defining and managing the quality execution of clinical studies. Partner closely with product and technology development to design and execute clinical studies for claims support, credentialing, decision making, and fundamental understanding. The CTM role is pivotal for driving robust human testing and clinical trials that are compliant with established governance principles, including ICH-GCP Guidelines. Responsibilities: Design, implementation, and management of clinical trials, Development of both external and internal networks for the integration of key components of a successful clinical trial. Management of study logistics, timelines, and budget/expense tracking.
- Prepare documentation for study placement and clearances, clinical trial protocols, and IRB submissions, as needed. Conduct study close-out and tasks, including documentation and archiving of study materials.
- Contribute to the development of Standard Operating Procedures and adhere to all aspects of Governance and Quality systems. Represent clinical operations are regulatory meetings, sponsor meetings, and any other multifunctional meetings, as needed.
Qualifications:
- Experience in human testing and the management of Clinical Trials, including a fundamental knowledge of Good Clinical Practices.
- The candidate will have a strong background in a fundamental knowledge of Biology, Chemistry and/or measurement science.
If this job is a match for your background, we would be honoured to receive your application!
Providing consulting opportunities to TALENTed people since 1987, we offer a host of opportunities, including contract, contract to hire, and permanent placement. Let's talk
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