TRABAJO GLOBAL REGULATORY SUBMISSIONS PROJECT

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

regulatory efficacy expert – global leader... launch your european regulatory career with a growing global leader!... collaborate effectively with product development...

Perform/support submissions activities to swissmedic through the appropriate electronic gateway and support client during the entire regulatory process...

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

The candidate will lead all regulatory submissions... broad understanding of the evolving clinical landscape in hematology/oncology own the overall development of...

The rid will work closely with therapeutic area (ta) vp, executive regulatory science directors, global regulatory leaders (grls) and regulatory affairs directors...

Lead iqvia regulatory thought leadership in concert with iqvia’s our global network of regulatory science and strategy experts provide leadership, strategic direction...

Monitor and evaluate the changes of local regulatory requirements and industry standards and provide regulatory intelligence to sea and global regulatory partners...

Demonstrated project management, organizational and planning skills... the senior specialist, regulatory publishing is responsible for publishing and preparation...

Research, draft, circulate for cross-functional review and approval, and submit global regulatory affairs submissions...   primary responsibilities will include:...

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

Specialized focus on digital regulatory science, clinical medical affairs, pv (pharmacovigilance), sustainability, and other science-related project activities...

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...

Provide input to line managers of their project team members’ performance relative to project tasks... understand project strategy and operationalise the agreed...

Clinical project leads run their own studies... \u provide input to line managers of their project team members' performance relative to project tasks...

Collaborate with regional and global regulatory teams to align strategies and share best practices... provide support and guidance to the baltic regulatory team...

Excellent knowledge of study execution, benefit risk management and regulatory affairs... in addition, the gmal will be accountable for the global publications plans...

External/ internal reviews and investigations: provide support to the business, other relevant control functions and the regulatory management function with the...