TRABAJO GLOBAL REGULATORY SUBMISSIONS PROJECT

Provide regulatory guidance and support to project teams throughout the implementation process... are you passionate about regulatory compliance, business growth...

External core interactions with: regulatory authorities, cros, consultants, partners... champions use of expedited regulatory pathways globally to accelerate patients’...

Oversees the preparation and maintenance of regulatory submissions and files... provides guidance to project team members regarding regulatory compliance issues...

Prepares and/or reviews regulatory documents to support clinical trial submissions... investigational medicinal product dossier, clinical trial justifications may...

A project management professional (pmp) certificate is desirable... project manager, vaccines project services iqivia laboratories home-based, office-based, hybrid...

Johnson & johnson innovative medicine is recruiting for post-doctoral – global regulatory affairs scholar... global regulatory affairs (gra) is looking for a high...

regulatory certification (rac) preferred... project management certification preferred... project management experience leading global regulatory teams in a matrix...

regulatory submissions & documentation:prepare and review high-quality cmc sections for regulatory submissions (ind/impd, bla/nda, maa, variations/supplements)...

Experience with medical device regulatory new product submissions required... q-submissions, ides, de novo, 510(k)s) and global health authorities’ submissions technical...

The role will work on several regulatory software applications that leverage the connected regulatory intelligence platform... pharma product manager - connected...

Medtech business analyst - connected regulatory intelligence the iqvia connected regulatory intelligence (cri) is a groundbreaking innovative solution that simplifies...

Pharma business analyst - connected regulatory intelligence the iqvia connected regulatory intelligence (cri) is a groundbreaking innovative solution that simplifies...

Experience with medical device regulatory new product submissions required... prepares and submits regulatory information required to obtain global market access...

Experience with project controls processes... understanding of complex technical and regulatory issues impacting products... the pmo lead will drive innovation to...

• provide input to line managers on their project team members’ performance relative to project tasks... understand project strategy and operationalise the agreed...

The project manager is responsible for maintaining the proper project documentation and ensuring compliance with sops and regulatory requirements for clinical...

Knowledge of global regulations, regulatory timelines, guidelines, and regulatory requirements related to marketing applications is required...

Excellent project planning and project management skills and experience with project management tools... engaging with industry associations and consortia, regulatory...

 provide expertise and support project planning, project management and implementation of functional initiatives to improve processes...   -provide updates/reports...

Ensure the conformity of related regulatory quality documents (process and procedures) and participate to their global continuous improvement... information managementparticipate...