
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.
🔥 18 hours ago
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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 and contractual terms within approved parameters • Ensure compliance with negotiation parameters, approvals, contractual processes, budgetary guidance, templates, and client expectations • Coordinate with internal functional departments to align site startup and contractual activities with agreed timelines • Align contract negotiations 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 tracking and reporting and 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 that 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 risk 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 15-20 lbs • Regular and consistent attendance
Apply Now🕒 Yesterday
Site Contract Specialist supporting clinical trial budgets, agreements, and investigator grants for global CRO PSI. Home-based in Mexico, collaborating with legal and study startup teams.
🗣️🇪🇸 Spanish Required
🕒 September 3
Site Contract Specialist supporting clinical research start-up projects for a global medical research CRO. Reviewing budgets, negotiating trial agreements, and coordinating site contracts across Latin America.
🗣️🇪🇸 Spanish Required