TRABAJO REGULATORY SUBMISSIONS
(72 ofertas de trabajo)
Listado de trabajos de Regulatory submissions
Associate director, regulatory submissions project management
The associate director – regulatory submissions is responsible to lead a worldwide regulatory submissions delivery team within iqvia translations...
Regulatory affairs manager - (swiss submissions, home-based) (m/w/d)
Perform/support submissions activities to swissmedic through the appropriate electronic gateway and support client during the entire regulatory process...
Regulatory manager, clinical trials regulatory management- home-based, europe
Prepares and/or reviews regulatory documents to support clinical trial submissions... independently provides regulatory support for complex projects and programs...
Regulatory affairs associate manager
Liaise and establish cooperative relationships with source company regulatory colleagues to ensure understanding of regulatory requirements in singapore and request...
Senior regulatory affairs specialist
Eu, and israel cmc-related regulatory filings... research, draft, circulate for cross-functional review and approval, and submit global regulatory affairs submissions...
Regulatory affairs associate xiromed
General responsibility manages new regulatory submissions and assisting with the lifecycle management of the existing portfolio, ensuring alignment of regulatory...
Responsibilities:manages a team of regulatory affairs employees... oversees resource assignments and participates in the preparation, review, submission, maintenance...
Regulatory and start up manager (sam)(fsp)
Determine regulatory strategy/expectations and parameters for submissions and all necessary authorizations... provide specialist regulatory and technical scientific...
Associate manager, clinical trials regulatory management (m/w/d) - home-based, europe
Deliver regulatory training/presentations as required... prepares and/or reviews regulatory documents to support clinical trial submissions...
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Regulatory and start up specialist (fsp)
Prepare site regulatory documents, reviewing for completeness and accuracy... at least 1 years' experience with submissions and ctis experience...
Regulatory and start up specialist (fsp)
Prepare site regulatory documents, reviewing for completeness and accuracy... at least 1 years' experience with submissions and ctis experience...
As regulatory professionals working on oncology products, we work in areas of unmet need and take innovative regulatory approaches to bring life-changing treatments...
Overviewing the supporting detail as necessary for regulatory submissions, variations and renewals to strict deadlines... developing and managing a database for...
The role is responsible to support and facilitate the regulatory affairs activities to ensure that products comply and meet medical device regulatory requirementshttps://www...
Global clinical development scientist director - vaccines and immune
Provide expert scientific input into the preparation of regulatory documents and interactions with regulatory authorities... desirable experience with regulatory...
With access to our extensive capabilities and comprehensive pipeline, you’ll be involved in countless submissions and a wide range of engaging projects along the...
Sr. clinical research associate (spain)
Collect and review regulatory documents as required... may be required to manage the preparation of local clinical trial applications (for regulatory submissions...
Director, principal patient safety scientist
Leads safety strategy for regulatory submissions of new products, formulations or indications (nda/bla, maa), in partnership with the gsp and other functional experts...
Associate director, clinical project scientist (oncology)
ability to work 5 days a week fluent in written and spoken english working knowledge of the use of microsoft suite of software products including excel and...
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