
10,000+ employees
Founded 1956
🏥 Healthcare
📦 Logistics
🏭 Manufacturing
Healthcare • Logistics • Manufacturing
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
🏥 Healthcare
📦 Logistics
🏭 Manufacturing
Healthcare • Logistics • Manufacturing
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.
• Draft, review, negotiate and finalize amendments and budgets with study sites • Negotiate investigator grant budgets, contractual terms and conditions within approved parameters • Ensure compliance with negotiation parameters, authority approvals, contractual processes, client expectations, budgetary guidance, templates and procedures • Coordinate with internal functional departments to align site startup and contractual activities with agreed timelines • Ensure contract negotiation activities align with the critical path for site activation • Achieve target cycle times for site activations • Escalate out-of-parameter issues according to established guidelines and processes • Complete required tracking and reporting • Assist other specialists with tracking and reporting
• 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 0-2 years) • Basic understanding of clinical trial agreements • Basic ability to apply basic principles of investigator grant negotiation • General understanding of business and financial principles related to service agreements • Effective communication skills (verbal & written) in English and local language • Strong attention to detail • Excellent analytical and decision-based thinking • Able to work independently or in a team environment • Good organizational and time management skills • Working knowledge of PPD SOP & WPDs • Able to organize competing priorities logically and review outstanding contractual risks and issues • Able to effectively use automated systems and computerized applications • Ability to demonstrate a customer-focused style of communication, problem-solving and collaboration • Ability to work in an upright and/or stationary position for 6-8 hours per day • Ability to perform repetitive hand movements and frequent mobility • Ability to lift and carry objects up to 15-20 lbs • Regular and consistent attendance
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