TRABAJO CLINICAL ASSOCIATE SPAIN BARCELONA, BARCELONA

Essential skills/experience: relevant clinical or biomedical ph... job title: director clinical scientist, oncology r&d, early clinical location: barcelona, spain...

This role provides matrix management of functional area representatives to cross-functional clinical study teams... the exact accountabilities will differ depending...

The clinical regulatory writing associate director is expected to: • independently manage clinical regulatory writing activities across a portfolio of work...

€¢ *to acquire knowledge of ich gcp, the conduct of clinical trials and governing regulations, relevant icon sops, icon internal tracking systems and client sops...

Requirements: students of engineering, health sciences, etc with master’s degree in clinical trial monitoring / pharmaceutical industry... astrazeneca is an innovation-driven...

clinical trial insurance & ibm, manager     purpose: • manage clinical trial insurance process to globally achieve an appropriate insurance of clinical trials...

clinical trial posting expert     purpose: • supervise, manage and publicly disclose clinical trial information into clinical trial registries and disclosure...

Location: barcelona, spain (on-site) the global study associate director (gsad) is a business-critical role within study management r&d, development operations,...

The clinical cost analyst provides analysis and expertise about clinical studies financials to resource management at bayer pharma clinical operations...

  qualifications & competencies:   • degree in medicine, life sciences, or natural sciences or equivalent professional experience • experience...

Location: barcelona join our biopharmaceuticals r&d team as an associate director, study management... quality assurance, analytical, clinical and regulatory) to...

- 3 years experience in clinical trial disclosure with significant experience related to the conduct and analysis of clinical trials...     bayer welcomes applications...

  provision clinical study data to business consumers... knowledge of clinical data mapping, transformation and end to end processes... validation, report specifications...

Introduction to role: join our diverse team as a global study associate in haematology clinical operations... the global study associate is responsible for providing...

clinical study protocol (csp) through to clinical study report (csr)) in accordance with relevant az sops... this role is a key player within our study management...

) including other clinical trial applications... ) within studies   support implementation of data provisioning for usage in studies for clinical trial...

Independently planning and managing supply strategy for assigned clinical programs... main duties & responsibilities: the program manager will contribute directly...