
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.
🕒 April 24
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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.
• Responsible for end-to-end budget oversight from Clinical Study Protocol (CSP) development through study set-up, maintenance, close-out, and archiving. • Maintain the master study and country budgets, and drive timely distribution of approved country budgets to Site Management and Monitoring/country organizations. • Ensure application of country-level Fair Market Value (FMV) at study and country level. • Act as portfolio SMEs and primary POC for Clinical Study Agreements (CSAs) with SMM and Legal. • Coordinate deliverables across Study Teams, SMM, Legal, Procurement, Finance, and scientific functions; facilitate decision making, resolve issues, and drive alignment on budget and contract priorities and timelines.
• University degree (or equivalent) • At least 5 years of relevant clinical experience in the pharmaceutical industry, including 2+ years of site budget and contracts oversight/project management experience. • Extensive knowledge of clinical research regulatory requirements; excellent understanding of ICH/GCP, and study management processes, including contracting and study budget management. • Proven oversight/project management skills, including planning, risk management, timeline and budget oversight; proficiency with standard project tools and IT systems. • Strong organizational and problem-solving skills; ability to manage competing priorities and maintain attention to detail. • Fluent verbal and written English.
• Health insurance • 401(k) matching • Flexible work hours • Paid time off • Remote work options
Apply Now🕒 April 23
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