TRABAJO SCIENTIFIC REGULATORY AFFAIRS DIRECTOR BARCELONA, BARCELONA

The international regulatory affairs director (irad) is responsible for developing and implementing the international regulatory strategy for a group of products...

Represent regulatory affairs on global product teams (gpts) providing strategic advice and accountable for all regulatory activities... previous demonstrated experience...

• support individuals with regulatory knowledge at global and regional levels... this dynamic role combines line management, drug project leadership, and cross-project...

P rovide expert scientific input into the preparation of regulatory documents and interactions with regulatory authorities...   ensure scientific input to ta standards...

Provide expert scientific input into the preparation of regulatory documents and interactions with regulatory authorities... ensure scientific input to ta standards...

Summary location: london, uk or barcelona, spain role type: hybrid working, #li-hybrid as associate director (ad) scientific engagement governance you will be supporting...

• identify regulatory risks and propose mitigations to lead rpm and cross-functional teams... you'll be empowered to innovate, taking smart risks and breaking barriers...

Experience of global regulatory submissions and interacting with major regulatory agencies... clinical development, medical affairs, regulatory affairs)...

London, basel or barcelona role type: hybrid working, #li-hybrid the associate clinical development director (oncology)  (assoc... cdd) provides input to development...

In this pivotal role, you will help to channel our scientific capabilities to generate a positive impact and improve patients’ lives... we are driven by our determination...

This collaboration builds strategies to demonstrate and differentiate the value proposition and corresponding scientific evidence of alexion products for payers...

We are looking for an experienced individual in global drug development regulatory affairs to lead technical activities for the solutions that re-define how novartis...

), the job holder embeds global heor strategy into critical deliverables with the goal to demonstrate and differentiate the value proposition and corresponding scientific...

Medical research & development regulatory commercial etc... ) the job holder embeds global heor strategy into critical deliverables with the goal to demonstrate...

Responsibilities:implement translational medicine and early clinical development plans for different therapeutic candidatesdesign and implement clinical development...

Oversee the facility's biosafety management, ensuring adherence to established protocols, regulatory compliance, and promotion of a safe working environment...

•foster collaboration with key opinion leaders (kols) to support product evaluations and drive scientific publications... •coordinate and participate in key events...