Thermo Fisher Scientific
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.
Global Project Manager, FSP
Job not on LinkedIn
November 5
Thermo Fisher Scientific
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.
📋 Description
• Lead or support study operational strategy and planning and oversee execution of select clinical studies. • In close collaboration with various stakeholders, support or oversee the execution of select study/ies. • Oversee Strategic Partners and/or other CROs and other vendors to meet obligations. • Challenge study team to ensure operational feasibility and supports budget development. • Develop and manage study timelines and oversee trial risk and mitigation.
🎯 Requirements
• Bachelor’s Degree or international equivalent required; Life Sciences preferred. • Knowledge in global regulatory and compliance requirements for clinical research, including but not limited to US CFR, EU CTD, and ICH GCP. • Demonstrated successful experience in project/program management and matrix leadership. • 5+ years’ experience in pharmaceutical industry and/or clinical research organization, including 3+ years clinical study management/oversight. • Experience could include either early phase clinical studies or Phase 2 and 3 studies and global/international studies or programs. • Fluent business English (oral and written).
🏖️ Benefits
• Health insurance • 401(k) • Paid time off • Flexible work arrangements • Professional development
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