TRABAJO ASSOCIATE II REGULATORY SUBMISSIONS

The  associate director – regulatory submissions is responsible to lead a worldwide regulatory submissions delivery team within iqvia translations...

Liaise and establish cooperative relationships with source company regulatory colleagues to ensure understanding of regulatory requirements in singapore and request...

General responsibility manages new regulatory submissions and assisting with the lifecycle management of the existing portfolio, ensuring alignment of regulatory...

Prepares and/or reviews regulatory documents to support clinical trial submissions... deliver regulatory training/presentations as required...

The qa associate ii is responsible for providing quality assurance and quality oversight services to designated manufacturing sites... partner with qa document control...

Abiomed, part of johnson & johnson's medtech, is recruiting for a clinical research associate ii... trends in protocol compliance, enrollment, monitoring deviations...

We are looking for a clinical trail associate ii (ctaii) to join our a-team (hybrid*/remote)... as a ctaii at allucent, you act as the primary administrative support...

Responsibilities:manages a team of regulatory affairs employees... oversees resource assignments and participates in the preparation, review, submission, maintenance...

Clinical research associate (sr... collect and review regulatory documents as required... work with project manager (pm), clinical team leader (ctl) and/or lead...

Johnson & johnson is recruiting for an associate director, clinical project scientist, oncology...   ability to work 5 days a week fluent in written and...

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

Previous experience with regulatory submissions... collaborators, key opinion leaders (kols), investigators, regulatory authorities, etc... ability to travel...

Typical accountabilities   utilize physiologically-based pharmacokinetic (pbpk) and translational modeling tools to enable clinical pk projections for drug-drug...

Senior clinical research associate iqvia is the human data science company oriented to drive human health outcomes forward... your responsibilities will include:...

Why work with us?we are a global team making a difference in the world – our clinical trials improve the health of millions worldwidecompetitive salary and benefitsflexible...

Trains investigational site staff as necessary when applicable, supports preparation of regulatory and / or ec submissions qualifications college/university degree...

When applicable, supports preparation of regulatory and / or ec submissions...     i'm interested i'm interested privacy policy...   come and join us in this exciting...

Provide expert scientific input into the preparation of regulatory documents and interactions with regulatory authorities... experience particularly in phase ii...

Coordinating submissions... experience of overseeing cras, vendors and deliverables globally the ability to work effectively with a wide range of clinical, technical...