Senior Clinical Programmer I
¿Tiene su CV preparado? Si es así y confía en que este es el puesto ideal para usted, asegúrese de enviar su solicitud lo antes posible.
Location: Barcelona
Introduction to Role
The Senior Clinical Programmer I is primarily responsible for programming, dashboard development, and validation of data cleaning and review listings, as well as creating sophisticated programs for ongoing clinical studies.
Responsibilities
Design, develop, implement, and validate sophisticated programs built in Python, SAS, R, or SQL.
Develop and validate business‑intelligence solutions such as PowerBI and Spotfire dashboards.
Program independently with efficiency and quality to process, analyse and report clinical trial data for review by clinical study teams.
Lead high‑complexity projects or initiatives that are part of the clinical programming roadmap.
Define and build vital processes and tools for clinical programming activities at both global and study levels.
Contribute to the development of guidelines that enhance quality, efficiency, timelines, and effectiveness within the function.
Provide technical expertise and cross‑training to support the availability and performance of reports and dashboards for external and internal users.
Lead the completion of programming documentation to ensure activities are performed per standard operating procedures, guidelines, and protocols.
Ensure high quality is built into own work and in the work of other programmers.
Identify and communicate risks within assigned studies and/or projects.
Collaborate with teams including data management, development operations, clinical, biometrics, and other relevant multi‑functional teams to deliver end‑user reporting needs.
Develop and maintain data visualization tools, including requirement gathering, data provisioning, and dashboard building.
Create and maintain a catalogue of reports to aid data cleaning and reporting activities.
Essential Skills / Experience
Minimum of 5 years of professional experience and a bachelor’s degree.
Accomplished programming skills in Python, SAS, R, SQL, Power BI, Spotfire, or other dashboard technologies.
Intermediate knowledge of the clinical development process.
Good knowledge of industry standards and clinical programming guidelines.
Excellent analytical, critical thinking, written, and communication skills.
Ability to influence partners and work effectively in a distributed team environment.
Technical expertise with data capture, data models, data mining, and visualization techniques.
Prior experience and understanding of EDC systems such as Medidata Rave, Inform, Veeva, and data platforms like Saama, Entimice, SAS LSAF.
Desirable Skills / Experience
Master’s degree or equivalent in computer science, life science, or statistics.
Excellent collaborative skills and ability to manage complexity and change in a dynamic environment.
Broad knowledge of FDA regulations and GCP/ICH guidelines as they relate to clinical programming processes.
Experience producing analytical dashboards with Power BI, Spotfire, or other BI tools.
Knowledge of MicroStrategy.
AstraZeneca is an equal opportunity employer on the basis of race, color, religion, sex, national origin, age, sexual orientation, gender identity, status as a protected veteran, and status as a person with a disability. xhfqzwm Disabilities will be considered in a reasonable accommodation of the application, assessment, and selection processes. If you require a reasonable accommodation, please email
#J-18808-Ljbffr
or continue with email
¿Tiene su CV preparado? Si es así y confía en que este es el puesto ideal para usted, asegúrese de enviar su solicitud lo antes posible.
Location: Barcelona
Introduction to Role
The Senior Clinical Programmer I is primarily responsible for programming, dashboard development, and validation of data cleaning and review listings, as well as creating sophisticated programs for ongoing clinical studies.
Responsibilities
Design, develop, implement, and validate sophisticated programs built in Python, SAS, R, or SQL.
Develop and validate business‑intelligence solutions such as PowerBI and Spotfire dashboards.
Program independently with efficiency and quality to process, analyse and report clinical trial data for review by clinical study teams.
Lead high‑complexity projects or initiatives that are part of the clinical programming roadmap.
Define and build vital processes and tools for clinical programming activities at both global and study levels.
Contribute to the development of guidelines that enhance quality, efficiency, timelines, and effectiveness within the function.
Provide technical expertise and cross‑training to support the availability and performance of reports and dashboards for external and internal users.
Lead the completion of programming documentation to ensure activities are performed per standard operating procedures, guidelines, and protocols.
Ensure high quality is built into own work and in the work of other programmers.
Identify and communicate risks within assigned studies and/or projects.
Collaborate with teams including data management, development operations, clinical, biometrics, and other relevant multi‑functional teams to deliver end‑user reporting needs.
Develop and maintain data visualization tools, including requirement gathering, data provisioning, and dashboard building.
Create and maintain a catalogue of reports to aid data cleaning and reporting activities.
Essential Skills / Experience
Minimum of 5 years of professional experience and a bachelor’s degree.
Accomplished programming skills in Python, SAS, R, SQL, Power BI, Spotfire, or other dashboard technologies.
Intermediate knowledge of the clinical development process.
Good knowledge of industry standards and clinical programming guidelines.
Excellent analytical, critical thinking, written, and communication skills.
Ability to influence partners and work effectively in a distributed team environment.
Technical expertise with data capture, data models, data mining, and visualization techniques.
Prior experience and understanding of EDC systems such as Medidata Rave, Inform, Veeva, and data platforms like Saama, Entimice, SAS LSAF.
Desirable Skills / Experience
Master’s degree or equivalent in computer science, life science, or statistics.
Excellent collaborative skills and ability to manage complexity and change in a dynamic environment.
Broad knowledge of FDA regulations and GCP/ICH guidelines as they relate to clinical programming processes.
Experience producing analytical dashboards with Power BI, Spotfire, or other BI tools.
Knowledge of MicroStrategy.
AstraZeneca is an equal opportunity employer on the basis of race, color, religion, sex, national origin, age, sexual orientation, gender identity, status as a protected veteran, and status as a person with a disability. xhfqzwm Disabilities will be considered in a reasonable accommodation of the application, assessment, and selection processes. If you require a reasonable accommodation, please email
#J-18808-Ljbffr
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