📑 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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📑 Site Manager - 2406183712W **Description** Johnson & Johnson, through its operating companies, is the world's most comprehensive and broadly based manufacturer of health care products, as well as a provider of related services, for the consumer, pharmaceutical, and medical devices and diagnostics markets. We strive to provide scientifically s ...
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📑 Senior Local Trial Manager - 2406182759W **Description** We are looking for a driven **Senior Local Trial Manager (LTM)** to report to the Clinical Research Manager (CRM), running assigned clinical trials (phases 1b-2-3) in Belgium (Beerse) and The Netherlands (Breda). You will have operational oversight of assigned protocols from start-up t ...
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📑 **Join us in our exciting journey!!** **IQVIA is expanding in EMEA!!** We currently have a Regional CPM **to work sponsor-dedicated** to one of our pharmaceutical clients The Clinical Trial Manager (CTM) is accountable for the operational and scientific oversight, the set-up, execution and delivery of their assigned clinical trials ...
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📑 Senior Clinical Research Associate (Senior Site Manager) - 2406182788W **Description** A Senior Clinical Research Associate (Senior Site Manager) serves as the primary contact point between the Sponsor and the Investigational Site. A Senior Clinical Research Associate is assigned to trial sites to ensure inspection readiness through complianc ...
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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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📑 Internship GCO - 2406181372W **Description** Join us as a GCO intern to help advance the future of health – and follow a career with purpose. **Imagine The Breakthroughs We’ll Make Together** At Johnson & Johnson, we use technology and the power of teamwork to discover new ways to prevent and overcome the world’s the most significant he ...
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📑 **The Position** Biostatistics and Data Sciences (BDS) is a global organization with more than 400 employees within the Human Pharma Business Unit. Working in close collaboration with other functions at Boehringer Ingelheim (BI) and external vendors we combine methodological and technical data science skills with business and scientific expe ...
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📑 **The Position** Biostatistics and Data Sciences (BDS) is a global organization with more than 400 employees within the Human Pharma Business Unit. Working in close collaboration with other functions at Boehringer Ingelheim (BI) and external vendors we combine methodological and technical data science skills with business and scientific expe ...
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📑 **The Position** Biostatistics and Data Sciences (BDS) is a global organization with more than 400 employees within the Human Pharma Business Unit. Working in close collaboration with other functions at Boehringer Ingelheim and external vendors we combine methodological and technical data science skills with business and scientific expertise ...
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📑 **The Position** Biostatistics and Data Sciences (BDS) is a global organization with more than 400 employees within the Human Pharma Business Unit. Working in close collaboration with other functions at Boehringer Ingelheim and external vendors we combine methodological and technical data science skills with business and scientific expertise ...
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📑 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: Accountability & Delivery, Coll ...
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📑 ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development. The Clinical Trials Associate is responsible for assisting clinical study teams in ...
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📑 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: Accountability & Delivery, C ...
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📑 **Job Overview** Perform daily administrative activities, in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams, to ensure a complete and accurate Trial Master File delivery. **Essential Functions** • Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team with accurately updat ...
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📑 **Job Description** At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while t ...
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📑 **Job Description** At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while t ...
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📑 **Local Trial Manager** + Full time job + Contract with fixed period of 1 year with the possibility of extension for an indefinite period + The possibility of residence anywhere within the Czech Republic **Role purpose** + Primary point of contact to lead, manage and co-ordinate the conduct of clinical trials from study s ...
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📑 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: Accountability & Delivery, C ...
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📑 **Job Description** At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while t ...
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📑 Senior Clinical Research Manager - 2406176345W **Description** We are looking for a driven **Senior Clinical Research Manager** to join our growing Clinical Operations team in The Netherlands (Breda) and Belgium (Beerse). In this role, you will manage a team of Local Trial Managers (Local project managers), Site Managers (Clinical Research A ...
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📑 **Job Description** At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while t ...
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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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📑 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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Great News! We have discovered exciting live Trial scienti job opportunities in Europe just for you at European Jobs. You can even download the search results for Trial scienti jobs in europe here.
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There are currently 500 live jobs available for Trial scienti in Europe according to European Jobs.
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There is a wide range of job opportunities in Europe. The available jobs vary across industries and sectors, providing options for professionals with different skills and interests.
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There are currently 4,133,589 total jobs available in Europe according to European Jobs.