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.
Analytical Instruments β’ Laboratory Supply Chain Programs and eCommerce β’ Laboratory Equipment β’ Lab Services β’ Specialty Diagnostics
September 25, 2024
πͺπΊ Anywhere in Europe β Remote
β° Full Time
π’ Junior
π‘ Mid-level
π¨ββοΈ Medical Director
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.
Analytical Instruments β’ Laboratory Supply Chain Programs and eCommerce β’ Laboratory Equipment β’ Lab Services β’ Specialty Diagnostics
β’ Provide medical leadership to the study teams, including creating clinical trial protocols while implementing the latest scientific information. β’ Contribute to site selection, involved in review and approval of study protocols and amendments. β’ Ensure medical validity of each individual primary endpoint as well study subject safety. β’ Controls, handles and follows day to day activities during the course of the clinical trial.
β’ Significant experience within pharmaceutical industry, clinical trials and pharmaceutical medicine is critically important. β’ Is fluent in spoken and written English. β’ Shown understanding and experience with NDA submission process. β’ Shown understanding of regulatory guidelines for adverse event reporting. β’ Strong communication & presentation skills and is a strong teammate.
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