📑 **Role Overview:** _The Site Enablement Solutions team at IQVIA provides qualified, clinically experienced research staff to clinical trial sites globally to accelerate and optimize the performance of clinical trials. By supplying sites with support for data entry, patient recruitment, patient visits, assessments, and other tasks ...
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📑 **IQVIA Safety Operations** team play an important part in the design, build and execution of end-to-end safety solutions for major pharmaceutical companies and their post market products around the world. We are proud to be an international, diverse team based across the world, with ‘safety hubs’ in Ireland, Poland, Austria, Portugal, Slovakia, S ...
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📑 **IQVIA Safety Operations** team play an important part in the design, build and execution of end-to-end safety solutions for major pharmaceutical companies and their post market products around the world. We are proud to be an international, diverse team based across the world, with ‘safety hubs’ in Ireland, Poland, Austria, Portugal, Slovakia, S ...
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📑 **IQVIA Safety Operations** team play an important part in the design, build and execution of end-to-end safety solutions for major pharmaceutical companies and their post market products around the world. We are proud to be an international, diverse team based across the world, with ‘safety hubs’ in Ireland, Poland, Austria, Portugal, Slovakia, S ...
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📑 Prepares and/or reviews regulatory documents to support clinical trial submissions. Independently provides regulatory support for more complex projects. **RESPONSIBILITIES** + Acts as a Clinical Trial Regulatory Manager (CTRM) on global projects which may be complex + Ability to administratively and te ...
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📑 **JOIN US ON OUR EXCITING JOURNEY!** IQVIA™ is The Human Data Science Company™, focused on using data and science to help healthcare clients find better solutions for their patients. Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness advances in healthcare information, tech ...
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📑 Prepares and/or reviews regulatory documents to support clinical trial submissions. Independently provides regulatory support for complex projects and programs **RESPONSIBILITIES** + Acts as a Clinical Trial Regulatory Manager (CTRM) on complex clinical trial projects or programs and may act as a Regulatory Ove ...
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📑 IQVIA is looking to appoint statistical programmers to utilize the SAS programming language to develop clinical study report materials according to the objectives of a clinical trial for regulatory submissions. Programming and performing related tasks serving the full spectrum of statistical programming needs in our DS3 environment (home based):<br ...
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📑 Supply Chain and Procurement Associate Date: Apr 16, 2024 Location: Vilnius, Lithuania, 01100 Company: Teva Pharmaceuticals Job Id: 55312 **Who we are** Together, we’re on a mission to make good health more affordable and acces ...
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📑 **The Manager, Regulatory Affairs International supports ambitious geographical expansion plans. The position will support registration of existing portfolio products into new territories and to register several of development projects into the international region. This role is key to driving both the Regulatory strategy and execution.** **• Prov ...
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📑 **Job Description** **Are You Ready to Make It Happen at Mondelēz International?** **Join our Mission to Lead the Future of Snacking. Make It Matter.** As an **Associate Counsel Baltics** you will: + collaborate with all functions in Baltics countries on day-to-day matter ...
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📑 Teach English Online! + Stable Class Hours = Stable Income + Fixed Student & Teacher pairing + Long-term employment only! (1 year+) About YiYiEnglish: Since 2017, YiYiEnglish has ...
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📑 **It's fun to work in a company where people truly BELIEVE in what they're doing!** **Job Description Summary:** The Associate Technical Support Engineer assists Rocket customers with questions and problems regarding the installation, setup, configuration and functionality of Rocket Software products. The Engin ...
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