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IQVIA
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Reading,
United Kingdom
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project.
May be Project Manager/Project Lead for a major study or a series/group of studies ... , prioritizing , coaching and process execution.
Education
Bachelor's Degree: Clinical
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IQVIA
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Wilayah Persekutuan Kuala Lumpur,
Malaysia
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(Clinical Project Manager) with experience in Cardiovascular, Renal and Metabolic diseases to join our innovative and dynamic group.
The Clinical Project Manager / Senior Clinical Project Manager role
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IQVIA
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Shanghai,
China
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Clinical Project Leader/ Senior Clinical Project Leader
**Global Project Leadership ... , enabled by best-in-class technology and data analytics.
Key collaborators are the Clinical Lead for
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IQVIA
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Amsterdam,
Netherlands
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When you join us as a Sponsor dedicated Line Manager you will be responsible for efficient ... responsibilities.
Allocation of resources to clinical research projects by assigning employees to clinical
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IQVIA
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Belgrade,
Serbia
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technology and data analytics.
Key collaborators are the Clinical Lead for site management, the Project Vendor Manager, the Project Management Analyst for project coordination, tracking and financial
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IQVIA
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Centurion,
South Africa
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technology and data analytics.
Key collaborators are the Clinical Lead for site management, the Project Vendor Manager, the Project Management Analyst for project coordination, tracking and financial
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IQVIA
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Bratislava,
Slovakia
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technology and data analytics.
Key collaborators are the Clinical Lead for site management, the Project Vendor Manager, the Project Management Analyst for project coordination, tracking and financial
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IQVIA
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Bloemfontein,
South Africa
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technology and data analytics.
Key collaborators are the Clinical Lead for site management, the Project Vendor Manager, the Project Management Analyst for project coordination, tracking and financial
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IQVIA
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Madrid,
Spain
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technology and data analytics.
Key collaborators are the Clinical Lead for site management, the Project Vendor Manager, the Project Management Analyst for project coordination, tracking and financial
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IQVIA
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Brussels,
Belgium
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a Clinical Trial Regulatory Manager (CTRM) on complex clinical trial projects or programs and may ... Prepares and/or reviews regulatory documents to support clinical trial submissions. Independently
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IQVIA
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Tel Aviv,
Israel
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a Clinical Trial Regulatory Manager (CTRM) on complex clinical trial projects or programs and may ... Prepares and/or reviews regulatory documents to support clinical trial submissions. Independently
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IQVIA
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New Cairo,
Egypt
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a Clinical Trial Regulatory Manager (CTRM) on complex clinical trial projects or programs and may ... Prepares and/or reviews regulatory documents to support clinical trial submissions. Independently
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IQVIA
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Gothenburg,
Sweden
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a Clinical Trial Regulatory Manager (CTRM) on complex clinical trial projects or programs and may ... Prepares and/or reviews regulatory documents to support clinical trial submissions. Independently
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IQVIA
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Vienna,
Austria
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a Clinical Trial Regulatory Manager (CTRM) on complex clinical trial projects or programs and may ... Prepares and/or reviews regulatory documents to support clinical trial submissions. Independently
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IQVIA
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Frankfurt,
Germany
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a Clinical Trial Regulatory Manager (CTRM) on complex clinical trial projects or programs and may ... Prepares and/or reviews regulatory documents to support clinical trial submissions. Independently
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IQVIA
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Amsterdam,
Netherlands
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a Clinical Trial Regulatory Manager (CTRM) on complex clinical trial projects or programs and may ... Prepares and/or reviews regulatory documents to support clinical trial submissions. Independently
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IQVIA
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Oslo,
Norway
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a Clinical Trial Regulatory Manager (CTRM) on complex clinical trial projects or programs and may ... Prepares and/or reviews regulatory documents to support clinical trial submissions. Independently
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IQVIA
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Solna,
Sweden
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a Clinical Trial Regulatory Manager (CTRM) on complex clinical trial projects or programs and may ... Prepares and/or reviews regulatory documents to support clinical trial submissions. Independently
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IQVIA
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Paris,
France
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a Clinical Trial Regulatory Manager (CTRM) on complex clinical trial projects or programs and may ... Prepares and/or reviews regulatory documents to support clinical trial submissions. Independently
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IQVIA
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Ljubljana – Dunajska,
Slovenia
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a Clinical Trial Regulatory Manager (CTRM) on complex clinical trial projects or programs and may ... Prepares and/or reviews regulatory documents to support clinical trial submissions. Independently
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IQVIA
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Kiev,
Ukraine
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a Clinical Trial Regulatory Manager (CTRM) on complex clinical trial projects or programs and may ... Prepares and/or reviews regulatory documents to support clinical trial submissions. Independently
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IQVIA
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Centurion,
South Africa
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a Clinical Trial Regulatory Manager (CTRM) on complex clinical trial projects or programs and may ... Prepares and/or reviews regulatory documents to support clinical trial submissions. Independently
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IQVIA
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Madrid,
Spain
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a Clinical Trial Regulatory Manager (CTRM) on complex clinical trial projects or programs and may ... Prepares and/or reviews regulatory documents to support clinical trial submissions. Independently
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IQVIA
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Sofia,
Bulgaria
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a Clinical Trial Regulatory Manager (CTRM) on complex clinical trial projects or programs and may ... Prepares and/or reviews regulatory documents to support clinical trial submissions. Independently
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IQVIA
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Lisbon,
Portugal
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a Clinical Trial Regulatory Manager (CTRM) on complex clinical trial projects or programs and may ... Prepares and/or reviews regulatory documents to support clinical trial submissions. Independently
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IQVIA
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Prague,
Czech Republic
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a Clinical Trial Regulatory Manager (CTRM) on complex clinical trial projects or programs and may ... Prepares and/or reviews regulatory documents to support clinical trial submissions. Independently
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IQVIA
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Bellville,
South Africa
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a Clinical Trial Regulatory Manager (CTRM) on complex clinical trial projects or programs and may ... Prepares and/or reviews regulatory documents to support clinical trial submissions. Independently
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IQVIA
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Dublin,
Ireland
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a Clinical Trial Regulatory Manager (CTRM) on complex clinical trial projects or programs and may ... Prepares and/or reviews regulatory documents to support clinical trial submissions. Independently
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IQVIA
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Reading,
United Kingdom
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a Clinical Trial Regulatory Manager (CTRM) on complex clinical trial projects or programs and may ... Prepares and/or reviews regulatory documents to support clinical trial submissions. Independently
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IQVIA
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Belgrade,
Serbia
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a Clinical Trial Regulatory Manager (CTRM) on complex clinical trial projects or programs and may ... Prepares and/or reviews regulatory documents to support clinical trial submissions. Independently
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