TRABAJO GLOBAL REGULATORY SUBMISSIONS PROJECT

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

Also provides strategic regulatory input as requireddevelops and/or reviews documents intended for submission to the regulatory authorities and/or ethics committees...

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 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...

Ensures centralization of start-up global regulatory information and maintenance of the regulatory intelligence database... participates in regulatory watch activities...

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...

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...

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...

Support cls during project review meetings... manage the clinical team at project level to successfully deliver the project through the establishment of high-quality...

·       embrace change, continuous learning, and work skills improvement key responsibilities: ·      ...

This requires early anticipation of the potential regulatory impact and developing capabilities to design regulatory strategies applicable to late development projects...

Portfolio strategy: contribute to the broader therapeutic area strategy global commercialization strategy development: formulate and implement global commercialization...