Thermo Fisher Scientific
Thermo Fisher Scientific is the world leader in serving science, with annual revenue of more than $40 billion. Their mission is to enable customers to make the world healthier, cleaner, and safer by supporting life sciences research, solving complex analytical challenges, increasing laboratory productivity, and improving patient health through diagnostics and the development of life-changing therapies. With a global team, they offer innovative technologies and pharmaceutical services through brands such as Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services, Patheon, and PPD.
Analytical Instruments • Laboratory Supply Chain Programs and eCommerce • Laboratory Equipment • Lab Services • Specialty Diagnostics
Clinical Systems Operations Specialist
March 6
Thermo Fisher Scientific
Thermo Fisher Scientific is the world leader in serving science, with annual revenue of more than $40 billion. Their mission is to enable customers to make the world healthier, cleaner, and safer by supporting life sciences research, solving complex analytical challenges, increasing laboratory productivity, and improving patient health through diagnostics and the development of life-changing therapies. With a global team, they offer innovative technologies and pharmaceutical services through brands such as Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services, Patheon, and PPD.
Analytical Instruments • Laboratory Supply Chain Programs and eCommerce • Laboratory Equipment • Lab Services • Specialty Diagnostics
📋 Description
• Coordinate the quality control of study configurations in Clinical Trial Management Systems • Handles all elements of quality checks at a study level, including but not limited to understanding and following SOP’s and work instructions • Identifies, researches, and resolves technical problems • Ensures study configuration accurately represents protocol requirements, study budget, and site network needs • Liaises with study builders to ensure understanding of the build design and study requirements prior to undertaking QC activities
🎯 Requirements
• Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 3+ years) • Experience with ICH-GCP, FDA, and other regulatory guidelines • Experience of medical terminology, clinical research protocols, clinical study budgets/contracts, and study documentation is preferred • In-depth knowledge of study configuration processes • Excellent problem-solving abilities • Ability to work independently and keep up with rapid changes in priorities
🏖️ Benefits
• Competitive remuneration • Annual incentive plan bonus • Healthcare • A range of employee benefits
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