📑 Job Advert Posting At ICON, it’s our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfil our mission to advance and improve patients’ lives. Our ‘Own It’ culture is driven by four key values that bring us together as individuals and set us apart as an organisation: Ac ...
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📑 **Who We Are** At Kyndryl, we design, build, manage and modernize the mission-critical technology systems that the world depends on every day. So why work at Kyndryl? We are always moving forward – always pushing ourselves to go further in our efforts to build a more equitable, inclusive world for our employees, our customers and our communi ...
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📑 On behalf of a leading infrastructure group in Dublin, we are looking to hire a Group Tax Manager. In this role you will be responsible for the management of regular reporting on Group tax activities and provide tax support for the funding requirements for large-scale, onshore and offshore projects. Requirements Qualification in accountancy (ACA/AC ...
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📑 Do you want to support Radiometer’s vision to improve global healthcare with reliable, fast, and easy patient diagnoses? Do you have experience with electronic trial master files (eTMF) in clinical studies and a flair for structure and good documentation practices? Then you could be our next colleague in the team of Clinical Operations. ...
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📑 Clinical Trial Support Intern - 2406181687W **Description** Clinical Trial Support Intern Location: Sofia Duration: 12 months Sector: Pharma Type: part-time (20hours/week) / full time Working at Johnson & Johnson can change everything. Including YOU. For more than 130 years, diversity, equity & inclusion (DEI) have been part ...
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📑 **Who We Are** At Kyndryl, we design, build, manage and modernize the mission-critical technology systems that the world depends on every day. So why work at Kyndryl? We are always moving forward – always pushing ourselves to go further in our efforts to build a more equitable, inclusive world for our employees, our customers and our communi ...
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📑 **Job Description** Thermo Fisher Scientific Inc. is the world leader in serving science, with annual revenue of more than $40 billion. Our Mission is to enable our customers to make the world healthier, cleaner and safer. Whether our customers are accelerating life sciences research, solving complex analytical challenges, growing efficiency ...
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📑 Local Clinical Trial Manager / Local Trial Manager - 2406185055W **Description** The Local Trial Manager (LTM) is responsible for local management of a clinical trial (or Medical Affairs data generation activity) in a country or countries. The LTM is the primary point of contact at a country level for assigned studies and has operational over ...
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📑 IQVIA is hiring a Clinical Trials Coordinator (trilingual) to provide service to one of our sponsors a well known pharma company with offices in Brussels to support the submissions, budgeting, agreement and payments. **Your duties** + Tracking (e.g. essential documents) and reporting (e.g. Safety Reports) + Ensure collation and dis ...
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📑 Wenn Sie Teil von Thermo Fisher Scientific sind, leisten Sie spannende Arbeit und werden Teil eines Teams, das Wert auf Leistung, Qualität und Innovation legt. Als Teil einer erfolgreichen, wachsenden globalen Organisation werden Sie ermutigt, Höchstleistungen zu erbringen. Mit einem Umsatz von rund 42 Milliarden US-Dollar und der größten Investiti ...
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📑 **Group Purpose** To facilitate product development and global registration by developing and executing regulatory strategies and effective regulatory agency interactions for product manufacturing and quality programs throughout product lifecycle. **Job Summary** The RA CMC Sr. Mgr. supports ADL Site and is responsible for prov ...
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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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📑 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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📑 Für den Bereich Manufacturing & Engineering suchen wir einen Production Operator (x|w|m) für die Sartorius Xell GmbH. In dieser Position produzieren Sie Flüssigmedien für Zellkulturen, die bei Gentherapien und Impfstoffen zum Einsatz kommen. Das Team freut sich darauf, mit Ihnen die Zukunft zu gestalten. Der Job erfolgt vor Ort in Schloss Holte-Stu ...
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📑 Für den Bereich Manufacturing & Engineering suchen wir einen Production Operator (x|w|m) für die Sartorius Xell GmbH. In dieser Position produzieren Sie Pulvermedien für Zellkulturen, die bei Gentherapien und Impfstoffen zum Einsatz kommen. Das Team freut sich darauf, mit Ihnen die Zukunft zu gestalten. Der Job erfolgt vor Ort in Schloss Holte-Stuk ...
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📑 Wenn Sie Teil von Thermo Fisher Scientific sind, leisten Sie spannende Arbeit und werden Teil eines Teams, das Wert auf Leistung, Qualität und Innovation legt. Als Teil einer erfolgreichen, wachsenden globalen Organisation werden Sie ermutigt, Höchstleistungen zu erbringen. Mit einem Umsatz von rund 42 Milliarden US-Dollar und der größten Investiti ...
🔗 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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📑 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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📑 Senior Clinical Research Associate (Senior Site Manager) - 2406173665W **Description** We are looking for a driven Senior Site Manager (Clinical Research Associate) to serve as the primary contact point between the Sponsor and the Investigational Site for trials in Late Development (phase 1b-2-3). As Senior Site Manager, you will be assigned ...
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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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