
10,000+ employees
Founded 1956
🧬 Biotechnology
đź’Š 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.
🔥 2 hours ago
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10,000+ employees
Founded 1956
🧬 Biotechnology
đź’Š 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.
• Draft, review, negotiate and finalize agreements with study sites • Negotiate investigator grant budget negotiation parameters, contractual terms and conditions • Ensure compliance to established negotiation parameters, authority approval, and client expectations • Identify and assess legal, financial and operational risks • Provide recommendations and alternative resolutions to Investigator Contracts negotiations • Coordinate with internal functional departments to ensure various site startup activities are aligned with contractual activities • Achieve target cycle times for site activations • Complete tracking and reporting as required • May provide training and mentoring to junior staff • Participate in country process improvement initiatives • Act as country subject matter expert in review of Investigator Contracts training materials • Liaise with Global Site Contracts to ensure compliance with established global processes
• 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 5+ years) • Detailed understanding of the principles of contract law • Effective communication skills (verbal & written) in English and local language • Detailed understanding and demonstrated ability to effectively negotiate investigator grant budgets • Strong attention to detail • Excellent analytical and decision based thinking skills • Solid knowledge and understanding of the pharmaceutical product development process and involvement of CROs • Able to work independently or in a team environment • Good organizational and time management skills • Working knowledge of PPD SOP & WPDs • Strong problem solving skills that are demonstrated via solid risk analysis that results in resolution or escalation as appropriate
• Health insurance • Professional development opportunities • Flexible working arrangements
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