TRABAJO DIRECTOR CLINICAL TRIAL MANAGEMENT BARCELONA, BARCELONA

What you’ll do the global clinical operations program director (gpd) is a core global role within the haematology  r&d clinical operations function...

Key member of  the clinical study team...   participating in safety review meeting regarding potential safety events within a given clinical study or ac ross the...

The clinical regulatory writing director provides expert communications leadership for the most complex and business-critical clinical activities by driving strategic...

The translational medicine (tm) oncology drug project management group at astrazeneca (az) is responsible for project and portfolio management to ensure the successful...

Desirable relevant clinical or biomedical ph... the clinical scientist is the link between the project team and all external clinical research for the program...

Delegation of authority, sunshine act, accord attestations, clinical trial transparency)... phd, msc program management certification... extensive knowledge of clinical...

• superior organizational and time management skills, facilitating efficient workflow and project management... • expertise in designing, planning and costing clinical...

  value added: the clinical project support specialist role is important for the clinical trials conduct by ensuring operational excellence and compliance...

You will be responsible for: providing support to the local study team in com in achieving quality and timeliness of study deliverables across the lifecycle of assigned...

The role holder will transform real-world clinical data into concrete insights for clinical development using statistical methods and innovative data visualizations...

We would prefer for you to have: · scientific degree of a clinical nature · experience in training instructional design and content management · medical affairs...

Solid knowledge of clinical trial data, and experience in analyzing and interpreting clinical trial data is required... collaborates with biostatistics team to work...

At least 2+ years of clinical experience post-registration... you will proactively evaluate the clinical implications of safety data from pre-clinical studies, clinical...

Thorough technical understanding of quality system, clinical trial process collecting, analyzing, and monitoring of third-party key quality indicators experience...

• responsible for patient safety document management (psdm) support, training, and qc (monthly and quarterly)... • acts as the interface between az portfolio & capacity...

Significant experience interpreting clinical data and collaborating with statisticians to deliver trial analyses required to parameterise health economic models...

We'd love to hear from you! the project manager, trial interactive is responsible for the management of implementation, maintenance and ongoing services for clients...

The global msl excellence director for oncology is accountable for ensuring the strategic alignment of msl activities and the development, delivery and reporting...

Support testing and verification of fair data management systems in collaboration with az stakeholders... analyse and interrogate multi-omics biomarker signatures...

With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our ppd clinical research portfolio, our...