
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.
🔥 1 hour 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 agreements with clinical study sites • Negotiate investigator grant budgets, contractual terms and conditions within approved parameters • Ensure compliance with negotiation parameters, approvals, contractual processes, client expectations, budget guidance, templates and procedures • Identify and assess legal, financial and operational risks and escalate issues appropriately • Provide recommendations and alternative resolutions for investigator contract negotiations • Coordinate with internal functional departments on site startup activities and contractual timelines • Align contract negotiations with the critical path for site activation • Achieve target cycle times for site activations • Escalate out-of-parameter issues through established channels • Liaise with study sites and internal functional teams to establish effective relationships • Ensure quality, objectivity and risk analysis in contract delivery
• Bachelor's degree or equivalent and relevant formal academic / vocational qualification • 2-5 years of previous relevant experience • Combination of appropriate education, training and/or directly related experience may be considered as an equivalency • Good understanding of contract law, including business, intellectual property, local tax and stamp laws • Ability to apply basic principles of investigator grant negotiation • General understanding of business and financial principles related to service agreements • Effective verbal and written communication skills in English and the local language • Ability to draft and negotiate contract provisions and budgetary issues within parameters with appropriate oversight • Attention to detail • Excellent analytical and decision-based thinking skills • Understanding of pharmaceutical product development and CRO involvement • Ability to work independently or in a team environment • Good organizational and time management skills • Working knowledge of PPD SOPs and WPDs • Ability to organize competing priorities and review contractual risks and issues • Ability to use automated systems and computerized applications • Customer-focused communication, problem-solving and collaboration skills • Ability to work upright and/or stationary for 6-8 hours per day • Ability to perform repetitive hand movements • Frequent mobility, bending, twisting, crouching and stooping • Ability to lift and carry 15-20 lbs • Ability to access and use computer software • Ability to communicate and understand spoken and written information • Ability to perform under stress, multitask and maintain regular attendance
• Fully remote work arrangement • Standard Monday-Friday work schedule
Apply Now🕒 September 8
Site Contract Specialist supporting clinical trial budgets, agreements, and investigator grants for global CRO PSI. Home-based role serving Latin American study startup operations in Colombia.
🗣️🇪🇸 Spanish Required