
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.
🕒 May 26
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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.
• Accountable for the operational delivery of clinical study/studies to time, quality, and budget • Support decision-making and lead study team to achieve overall study deliverables • Proactively identifies, oversees, and mitigates study risks • Ensures appropriate stakeholder communication regarding study status, expectations, risks and issues • Operate within the study budget • Leads investigator meetings and other study related meetings • Oversees activities of countries participating in the study
• Bachelor’s degree in life sciences or related discipline • At least 5+ years of relevant study management experience on a global level • In-depth experience in clinical research: study management, monitoring, data management • Previous in-depth Oncology experience • Experience from study feasibility to CSR • Proven experience from Ph II and PIII studies • Cross-functional leadership skills • Ability to input in clinical protocol, ICF, and other study plans • Strong experience in clinical budget management • Strong experience with vendor management including CRO • Exposed to competent authority Inspections (FDA, EMA, MHRA, PMDA...)
• Health insurance • Reasonable accommodations for individuals with disabilities • Professional development opportunities
Apply Now🕒 May 7
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