TRABAJO SAFETY MANAGER CLINICAL TRIALS

You will join a dynamic and international team of other european clinical development directors that work as part of the global clinical development (gcd) group...

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

Ensure clinical safety science contribution is aligned with regulations...   ensures input of suitable medical safety and clinical evidence expertise to the samd...

They are looking for a clinical affairs program manager europe... additional responsibilities include management of clinical trials approvals with local irbs and/or...

Responsibilities include: supports activities related to the design, execution, monitoring, and reporting of clinical trials... the clinical scientist provides active...

Previous clinical experience post-registration... experience of supervising patient safety colleagues... you will provide consistent communication of safety topics...

In-depth knowledge of applicable international guidelines regarding data management of clinical trials... johnson & johnson is currently seeking a senior clinical...

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

Demonstrated capability to consistently deliver clinical trials... senior clinical research associate will partner with the local trial manager (ltm), clinical trial...

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

• superior clinical research operational knowledge... clinical trial management and central trial oversight services provide for the regional/global coordination...

Comprehensive knowledge of clinical trial phases (phase i-iv)... demonstrated experience managing trials in europe (eu-wide experience essential)...

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

Pharmacovigilance), clinical research, or regulatory affairs solid knowledge in drug safety related processes (incl... supports all clinical trial activity and post...

Participate in monitoring study safety... able to manage complex and/or large trials... as a senior clinical trial manager you will be joining the world’s...

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

Participate in monitoring study safety... experience in executing a wide range of clinical trial activities (from initiation to clinical study report)...

Working as a senior clinical vendor manager at parexel fsp offers tremendous long-term job security and prospects... parexel is currently seeking a senior clinical...

Job description in line with current eurofins terminology, eurofins clinical diagnostics business in spain requires an itist manager (information technology infrastructure...