📑 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 technically/scientifically revie ...
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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 technically/scientifically revie ...
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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 technically/scientifically revie ...
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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 technically/scientifically revie ...
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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 technically/scientifically revie ...
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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 technically/scientifically revie ...
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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 technically/scientifically revie ...
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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 technically/scientifically revie ...
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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 technically/scientifically revie ...
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📑 **Senior Clinical Research Associate** IQVIA is the Human Data Science Company oriented to drive human health outcomes forward. When you join **IQVIA Bratislava** as a sponsor-dedicated CRA, you’ll enjoy the stability and resources of a leading, global contract research organization while gaining direct experience with one of our cu ...
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📑 **Senior Clinical Research Associate** IQVIA is the Human Data Science Company oriented to drive human health outcomes forward. When you join **IQVIA Zagreb** as a sponsor-dedicated CRA, you’ll enjoy the stability and resources of a leading, global contract research organization while gaining direct experience with one of our custom ...
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📑 **Senior Clinical Research Associate** IQVIA is the Human Data Science Company oriented to drive human health outcomes forward. When you join **IQVIA Sofia** as a sponsor-dedicated CRA, you’ll enjoy the stability and resources of a leading, global contract research organization while gaining direct experience with one of our custome ...
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📑 **Senior Clinical Research Associate** IQVIA is the Human Data Science Company oriented to drive human health outcomes forward. When you join **IQVIA Prague** as a sponsor-dedicated CRA, you’ll enjoy the stability and resources of a leading, global contract research organization while gaining direct experience with one of our custom ...
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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 Oversight for a key custome ...
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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 Oversight for a key custome ...
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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 Oversight for a key custome ...
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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 Oversight for a key custome ...
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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 Oversight for a key custome ...
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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 Oversight for a key custome ...
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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 Oversight for a key custome ...
🔗 View Salary and Additional Details 🎯 Get Your Ai Resume Score for this Job
📑 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 Oversight for a key custome ...
🔗 View Salary and Additional Details 🎯 Get Your Ai Resume Score for this Job
📑 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 Oversight for a key custome ...
🔗 View Salary and Additional Details 🎯 Get Your Ai Resume Score for this Job
📑 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 Oversight for a key custome ...
🔗 View Salary and Additional Details 🎯 Get Your Ai Resume Score for this Job
📑 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 Oversight for a key custome ...
🔗 View Salary and Additional Details 🎯 Get Your Ai Resume Score for this Job
📑 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 Oversight for a key custome ...
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📑 **Job Overview** Direct and manage the delivery of all required site activation, maintenance and regulatory activities for selected studies or multi-protocol programs, including pre-award activities, oversight of the scope of work, budget and resources. **Essential Functions** + Oversee the execution of Site Activation (including p ...
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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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📑 **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 ...
🔗 View Salary and Additional Details 🎯 Get Your Ai Resume Score for this Job
📑 **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 ...
🔗 View Salary and Additional Details 🎯 Get Your Ai Resume Score for this Job
📑 **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 ...
🔗 View Salary and Additional Details 🎯 Get Your Ai Resume Score for this Job
📑 **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 ...
🔗 View Salary and Additional Details 🎯 Get Your Ai Resume Score for this Job
📑 **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 ...
🔗 View Salary and Additional Details 🎯 Get Your Ai Resume Score for this Job
📑 **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 ...
🔗 View Salary and Additional Details 🎯 Get Your Ai Resume Score for this Job
Great News! We have discovered exciting live Regulatory iqvia job opportunities in Europe just for you at European Jobs. You can even download the search results for Regulatory iqvia jobs in europe here.
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There are currently 3,165,163 total jobs available in Europe according to European Jobs.