TRABAJO CLINICAL REGULATORY MANAGER

Prepares and/or reviews regulatory documents to support clinical trial submissions... independently provides regulatory support for complex projects and programs...

We are currently recruiting for a clinical director oncology (principal scientist) to join our european clinical development (ecd) team... the fastest way to breakthrough...

May conduct clinical audits of sponsor oversight, clinical investigator sites, clinical vendors, or clinical processes... inspections prepares the team and hosts...

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

Provides input to the clinical development plan, works on the development of the clinical trial protocol, clinical trial materials, supports completion of clinical...

They are looking for a clinical affairs program manager europe... overall responsibility for design of clinical trials including protocol development, clinical trial...

Drive knowledge management by sharing case studies/lessons learned from regulatory activities within the regulatory science & execution...

포지션: clinical sales manager – heart recovery 2... clinical support and in-service training: 1... complete the same clinical training as clinical specialists, ensuring...

The manager/associate director clinical pharmacology lifecycle management will provide clinical pharmacology, therapeutic and regulatory support for gsk’s product...

Collaborate with global cross-functional teams and the global regulatory affairs (gra) function/teams to facilitate regulatory activities... minimum 5 years of pharmaceutical...

Johnson & johnson is currently seeking a senior clinical data manager located in raritan, nj... strong clinical data management experience and/or knowledge of scientific...

The clinical it senior manager will collaborate with pmo leaders, clinical leaders, it teams, and other stakeholders to drive innovation and maintain the highest...

Arranges for the appropriate destruction of clinical supplies... 1-2 years of clinical trial monitoring experience is preferred... some supervision from a more senior...

Review clinical narratives... author/review clinical contributions to clinical study reports (csrs) and clinical portions of regulatory documents (e...

Knowledge of clinical trials - knowledge of clinical trial conduct, and skill in applying applicable clinical research regulatory requirements i...

Facilitate training programs on regulatory requirements for employees... participate in strategic planning and provide regulatory guidance... our mission is to revolutionize...

Senior clinical research associate will partner with the local trial manager (ltm), clinical trial assistant (cta) and clinical trial manager (ctm) to ensure overall...

Monitor and track legislation, regulatory development and the external environment, including proactively researching policies impacting bat regulatory agenda...

It's through our creative ideas that we uncover innovative regulatory approaches and pathways... the role holder will contribute and lead the regulatory cmc components...