
10,000+ employees
Founded 1956
🧬 Biotechnology
💊 Pharmaceuticals
🔬 Science
Biotechnology • Pharmaceuticals • Science
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.
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10,000+ employees
Founded 1956
🧬 Biotechnology
💊 Pharmaceuticals
🔬 Science
Biotechnology • Pharmaceuticals • Science
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.
• Actively participate with project team members to meet project needs, projections and deadlines. • Oversee organization and accuracy of project documents. • Work with management on understanding departmental needs and improving processes. • Provide support for the study conduct, working directly with study monitor and study subjects. • Oversee data entry, source data QC, EDC data entry and EDC query resolution, lab data verification, subject eligibility status review and subject eligibility notification. • Liaise with Sites to ensure enrolment projections are understood and tracked against actuals, reviewing screen failure rates, protocol deviations, quality, timelines and budget.
• Bachelor's degree or equivalent and relevant formal academic / vocational qualification • Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 0 to 2 years) • Basic knowledge of Phase I processes and clinical study operations • Fundamental knowledge of FDA and EMEA regulations and ICH GCP guidelines • Basic computer skills with working knowledge of Microsoft Office applications • Time management and multi-tasking skills • Written and verbal communication skills • Ability to prioritize workload and adapt to changing study needs • Ability to act as a liaison between external and internal groups.
• Health insurance • Retirement plans • Paid time off • Remote work options • Professional development opportunities
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