📑 **PURPOSE** **Engage in company training program to gain knowledge and skills required to provide administrative support to projects in accordance with SOPs, policies, good clinical practices, and applicable regulatory requirements. Meeting quality and timeline metrics under direction of line manager and/or other designated team members.** ...
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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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📑 Location: Portugal or Brazil At IQVIA, we look for the very best people, and then give them meaningful work to do. We don’t simply think about careers, we think about contributions. Those who choose to work with us are joining a recognized global leader – a company uniquely positioned to help clients make the most of market opportunities and ...
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📑 Location: Portugal or Brazil At IQVIA, we look for the very best people, and then give them meaningful work to do. We don’t simply think about careers, we think about contributions. Those who choose to work with us are joining a recognized global leader – a company uniquely positioned to help clients make the most of market opportunities and ...
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📑 Location: Portugal or Brazil At IQVIA, we look for the very best people, and then give them meaningful work to do. We don’t simply think about careers, we think about contributions. Those who choose to work with us are joining a recognized global leader – a company uniquely positioned to help clients make the most of market opportunities and ...
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📑 **Job Overview** **Manage the execution of the assigned clinical study (ies) from initiation through to closeout. Ensure that clinical study management and project deliverables are on time and is in accordance with standard operating procedures (SOPs), policies and practices. To provide project related support and assistance across multiple ...
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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 ...
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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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📑 **Primary Function:** **Centralized Monitoring Lead (CML)** **partners with the Clinical Lead and local country Site Monitors in project execution. Provides centralized support to monitoring visits and site management for a variety of protocols, sites and therapeutic areas. Monitors study start-up, manages resources, performs ongoing risk ...
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📑 We have great opportunities for those with a background working in Clinical Trials, preferably with a focus on patient recruitment/engagement, to join our Site and Patient Networks team. **PURPOSE** Assist Patient Recruitment Leads and manage assigned tasks related to the coordination, planning, and implementation of Patient Recruitme ...
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📑 We have great opportunities for those with a background working in Clinical Trials, preferably with a focus on patient recruitment/engagement, to join our Site and Patient Networks team. **PURPOSE** Assist Patient Recruitment Leads and manage assigned tasks related to the coordination, planning, and implementation of Patient Recruitme ...
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📑 We have great opportunities for those with a background working in Clinical Trials, preferably with a focus on patient recruitment/engagement, to join our Site and Patient Networks team. **PURPOSE** Assist Patient Recruitment Leads and manage assigned tasks related to the coordination, planning, and implementation of Patient Recruitme ...
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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, technology, anal ...
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📑 IQVIA™ – The Human Data Science Company™ – ist ein führender, globaler Anbieter von zukunftsweisender Analytik, Technologielösungen und klinischer Auftragsforschung. IQVIA unterstützt Life Science Unternehmen, Verbände, Institutionen, Kostenträger und weitere Akteure im Gesundheitswesen darin, bessere Ergebnisse in der Gesundheits-versorgung zu erz ...
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📑 IQVIA™ – The Human Data Science Company™ – ist ein führender, globaler Anbieter von zukunftsweisender Analytik, Technologielösungen und klinischer Auftragsforschung. IQVIA unterstützt Life Science Unternehmen, Verbände, Institutionen, Kostenträger und weitere Akteure im Gesundheitswesen darin, bessere Ergebnisse in der Gesundheits-versorgung zu erz ...
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