TRABAJO CLINICAL TRIALS ASSISTANT BARCELONA, BARCELONA

The ideal candidate will have extensive experience in cmo/cdmo environments, drug management, clinical operations, clinical trial supply chain management, bid defense...

Training / strong knowledge on good clinical practices... extensive knowledge of all steps included in a clinical trial... experience: 2-3 years of experience in...

Informática: dominio del paquete microsoft office a nivel de usuario avanzado, correspondencias, conocimientos y experiencia en el uso de herramientas estadísticas...

clinical input to nda/bla)... prepare and provide input to clinical study reports (csrs) and clinical portions of regulatory documents (e...

Typical responsibilities may include: •    provide long-range clinical planning in early clinical trial development, planning and managing of clinical research projects...

The key accountabilities will include driving components of or the whole clinical programme strategy for individual projects, as well as the overall concept and...

The exact accountabilities will differ depending on the exact nature of the clinical program so a high degree of flexibility and autonomy is required...

• disclose information on bayer s clinical trials at high level quality by fully complying to the related quality assurance processes...

Irb barcelona seeks a research assistant for the molecular modeling and bioinformatics group... the institute is devoted to conducting research of excellence in...

Irb barcelona is seeking an enthusiastic research assistant for the colorectal cancer laboratory led by dr... the institute is devoted to conducting research of...

  clinical trials data is a highly regulated and compliance driven environment...   provision clinical study data to business consumers...

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

If so, come and join us - iqvia are looking for a clinical research coordinator...   as a pivotal member of the site team, you will be involved with a variety of...

As a pivotal member of the site team, you will be involved with a variety of administrative tasks to support investigators and ensure the smooth running of clinical...

Excellent understanding of clinical trials methodology, gcp, gdmp and medical terminology... comprehensive knowledge of clinical standards, e...

Icon plc is a world-leading healthcare intelligence and clinical research organization... as a dmpm, you will manage a global team of clinical data management resources...

If so, come and join us - iqvia are looking for a clinical research coordinator... as a pivotal member of the site team, you will be involved with a variety of administrative...

Operational aspects of all clinical trial submissions made under the global/local clinical trial regulation pe eu ctr, in the clinical trial information system (ctis)...