TRABAJO ASSOCIATE II REGULATORY SUBMISSIONS

Johnson & johnson is recruiting for an associate director, cmc regulatory affairs... reviews cmc regulatory dossiers for global submissions throughout the product...

Collaborate with global regulatory teams and the global regulatory affairs (gra) function/teams to facilitate regulatory activities... the associate director, regulatory...

Experience in worldwide regulatory systems preferred... the regulatory affairs specialist ii provides regulatory guidance to project teams in business planning and...

Ability to author and submit us, eu and international regulatory submissions to regulatory bodies... partners with other functions to define and obtain data to assist...

The role reports to the associate director, regulatory operations & systems management... specific responsibilities regulatory systems compliance and managementensure...

We are currently seeking a study start up associate ii to join our diverse and dynamic team... study start up associate ii - german speaker icon plc is a world-leading...

We are currently looking for a french speaking site contract associate based in the emea region... the site contract associate is responsible for the coordination...

Strong understanding of regulatory requirements and guidelines for clinical trials, including ich-gcp and local regulatory requirements... in addition to your competitive...

Support accelerated regulatory filing activities across multiple regions/markets, with focus on country-specific requirements... lead the preparation, authoring...

The associate director drives decisions impacting document processing, establishes guidelines and standards, oversees resource allocation, and leads cross-functional...

• interact/collaborate with site management & monitoring, other internal staff, and external vendors in the collection of regulatory and other essential documents...

The associate director clinical scientist provides active scientific contribution to a cross-functional clinical team developing a molecular entity...

• work in close collaboration with the study-assigned cro (if applicable)  regulatory requirements support • assist in preparing ec/irb submissions and documents...

Provide strategic and operational clinical development expertise in interactions with regulatory and reimbursement authorities... contribute with high-quality scientific...

Demonstrate compliance with all applicable company, regulatory and country requirements... prepare, validate and submit regulatory documents such as completed iip...

regulatory reports, health authority responses and the safety content of marketing authorisation applications... we are looking for an experienced associate director...

Drive/contributing to clinical components of the ib, and documents for regulatory submissions and advisory requirements, including scientific advice, ind, eop2,...