Us To Apply

Healthcare

SeniorScientist,ClinicalIntelligenceEvidence

€65–95k ~AI est. Cuenca, Spain; Albacete, Spain FULL TIME
Market Sentiment
HIGH DEMAND

Neural analysis suggests this role is
optimal for Senior candidates.

The Brief

“Senior Scientist, Clinical Intelligence Evidence at Us To Apply. Skills: Epidemiology, Biostatistics, AI, Machine learning. Design observational studies. Deliver observational studies”

What You'll Achieve.

Address priority scientific questions; Address priority clinical development questions; Guide study design; Guide development milestones; Guide lifecycle decisions; Increase consistency; Increase efficiency

Industry & Context.

Healthcare
Problems you'll solve

Translate findings; Address scientific questions; Address clinical development questions; Implement statistical approaches; Implement comparative effectiveness; Implement longitudinal analysis; Implement causal inference; Implement patient characterization; Implement predictive analytics; Assess data suitability; Accelerate phenotyping; Accelerate endpoint identification; Accelerate workflow automation

What They're Looking For.

Must Have

Advanced degree in epidemiology, biostatistics, data science, public health, or related discipline, Understanding of observational study design, Understanding of epidemiologic methods, Understanding of real-world data interpretation, Experience applying machine learning or AI methods in healthcare data, Practical experience with real-world data assets, Experience applying quantitative methods to support evidence generation, Programming and data analysis skills in R, Python, and/or SQL, Ability to manage and deliver multiple analyses or projects, Advanced English

Nice to Have

PhD or MSc, Experience developing reusable analytical code, tools, or workflows, Familiarity with privacy-preserving analytics, Familiarity with federated approaches, Experience working across diverse data environments, Experience with multimodal real-world data, Experience with linked datasets, Experience in Cardiovascular, Renal and Metabolic (CVRM) disease areas

What You'll Do.

Design observational studies

Deliver observational studies

Address scientific questions

Address clinical development questions

Translate findings into recommendations

Guide development milestones

Guide lifecycle decisions

Conduct data feasibility

Implement statistical approaches

Implement comparative effectiveness

Implement longitudinal analysis

Implement causal inference

Implement patient characterization

Implement predictive analytics

Work across claims data

Work across electronic health records

Work across registries

Work across linked healthcare datasets

Assess data suitability

Deploy machine learning

Accelerate phenotyping

Accelerate endpoint identification

Accelerate workflow automation

Contribute reusable code

Scout new technologies

Evaluate new technologies

Adopt new technologies

Partner with Clinical Development

Partner with Biostatistics

Partner with Data Science

Communicate technical concepts

Uphold scientific quality

Uphold reproducibility

Follow documentation best practices

Follow coding best practices

Follow quality control best practices

Evolve team capabilities

Evolve team standards

How You'll Work.

Team & Collaboration

Cross-functional team; Clinical Development; Biostatistics; Data Science; Specialist audiences; Non-specialist audiences

Communication Scope

Explain technical findings; Communicate technical concepts

Process & Methodology

Manage projects, Deliver projects

Full Job Description

Are you ready to turn complex real-world data into evidence that shapes clinical development decisions in Cardiovascular, Renal and Metabolic disease? Join us to apply epidemiology, biostatistics and AI to answer high-value scientific questions that move medicines forward. In this role, you will be part of a cross-functional team bridging Clinical Development, Biostatistics and Data Science to design and deliver observational studies at scale. Your work will inform trial strategy, refine patient selection and endpoints, and improve the speed and quality of decision-making across the CVRM portfolio. Can you see yourself translating sophisticated analytics into clear, decision-relevant insights that influence the path of our pipeline? **Accountabilities:** * Evidence Generation and Study Delivery: Design and deliver observational studies and RWE projects that address priority scientific and clinical development questions across CVRM, from protocol and analysis plan through to results interpretation and dissemination. * Decision-Ready Insights: Translate findings into clear, evidence-based recommendations that guide study design, development milestones and lifecycle decisions. * End-to-End Analytical Execution: Build and validate cohort and phenotyping definitions; conduct data feasibility assessments; implement statistical analyses; and report results with transparency and reproducibility. * Scientific and Technical Expertise: Apply robust observational study design, epidemiology and biostatistics; select and implement approaches such as comparative effectiveness, longitudinal analysis, causal inference, patient characterization and predictive analytics aligned to the research question * Real-World Data Mastery: Work across claims, electronic health records, registries and linked datasets; assess suitability and limitations; and clearly document assumptions, methods and outputs aligned to internal scientific standards. * AI-Enabled and Scalable Analytics: Deploy AI an

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