Thermo Fisher Scientific
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.
Global Lead Project Manager – FSP
Job not on LinkedIn
🕒 April 4
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Thermo Fisher Scientific
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.
📋 Description
• Lead or support study operational strategy and planning and oversee execution of select clinical studies for assigned clinical program(s). • Support or oversee the execution of select study/ies in assigned clinical program(s) in compliance with quality standards. • Oversee Strategic Partners and/or other CROs and other vendors to meet the client obligations described in ICH-GCP and client business objectives. • Accountable for planning and operational strategy and execution for assigned clinical trials. • Provides subject matter expertise and operational input into protocol synopsis, final protocol and other study related documents. • Participates in country and site feasibility/selection process, with a focus on providing country insights, alignment and therapeutic expertise. • Develops and manages study timelines. • Supports/reviews study budget planning and management and accountable for external spend related to study execution.
🎯 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 E.g. timeline/budget management E.g. Risk identification and management. • 8+ years’ experience in pharmaceutical industry and/or clinical research organization, including 3+ years clinical study management/oversight. • 2+ years of experience in global lead project management field. • Oncology experience is required (as lead PM or Lead CTM). • Extensive ICF experience required (on a country and site level).
🏖️ Benefits
• Health insurance • 401(k) matching • Flexible work hours • Paid time off • Professional development opportunities
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