RWE Epidemiological Programmer - FSP (Oncology)

IQVIA LLC; City of Westminster; Presencial; GBP 60 000 - 90 000; Tempo integral

Resumo da oferta

IQVIA LLC is seeking a senior data analyst to lead the development of analytic datasets and longitudinal analyses for observational oncology studies using real‑world data (claims, EMR, and lab data). The role requires strong R programming skills, substantial experience with EMR/claims data, and a track record in safety analyses.

You will collaborate with epidemiologists and statisticians to design analyses, prepare protocols and reports, and manage multiple complex studies within the DATS

Qualificações

• Master’s Degree in Biostatistics, Epidemiology, Data Science or related field; 5–8 years of relevant experience or PhD with 3 years.
• Strong track record in real-world data analysis using claims, EMR and lab data; oncology safety experience preferred.
• Excellent statistical programming and ability to lead complex observational studies.

Responsabilidades

• Lead development of analytic datasets from raw data and perform data checks/cleaning.
• Feasibility assessment of real-world data sources to define patient cohorts and key variables.
• Conduct and QC analyses, apply statistical methods for censoring, confounding and missing data.
• Collaborate with epidemiologists to specify descriptive and complex statistics for oncology studies.
• Develop and QC study documents (protocols, SAPs, reports) using RWD (claims/EHR).
• Communicate timelines and results to project teams and stakeholders.

Conhecimentos

R programming

Observational study design

Pharmaceutical analytics

Data interpretation

Communication skills

Multi-task management

Formação académica

Master's degree in Biostatistics, Epidemiology, Data Science or related field

PhD in Biostatistics, Epidemiology, Data Science or related field

Ferramentas

Tempus

Flatiron

PharMetrics Plus

Descrição da oferta de emprego

• Lead development of analytic datasets through raw data processing and conduct data checks / cleaning using secondary real world data sources, including claims, EHR, and lab data (must have experience in PharMetrics Plus, Flatiron, or Tempus)
• Lead the feasibility of real-world data sources to characterize patient population, build patient cohorts, and define and validate key variables specific to study objectives.
• Conduct and QC analyses, identification of diagnosis and treatment codes and applying statistical methods to handle censor data, confounding, and missing data.
• Collaborate with epidemiologists to define specifications for descriptive and complex statistics (e.g., longitudinal analysis, survival analysis, regression models) in studies using RWD for oncology research questions, including safety analyses.
• Develop and QC TFLs for protocols/reports/manuscripts using RWD (e.g. claims and EHR)
• Support development of other study documents including protocols, statistical analysis plans, and study reports
• Communicate timelines, progress reports, and results to project team and key stakeholders
• Provide technical, programming, and statistical expertise and independently bring project solutions to team for complex studies
  It is important that this individual has prior experience in observational research utilizing EMR and claims data, particularly in safety analyses, along with a strong statistical programming skillset and experience managing multiple studies and complex analyses. In this role, individuals will have access to real-world databases and will act as stewards of the client's best practices, standards, and methodologies underlying the use of real-world data (RWD)., Master's Degree in Biostatistics, Epidemiology, Data Science or related field with 5-8 years relevant experience or PhD with 3 years relevant experience
• Strong track record of analysis of RWD using claims, EMR, and lab data (Tempus, Flatiron or PharMetrics Plus is preferred)
• Experience analyzing oncology data and safety outcomes is preferred.
• Demonstrated proficiency in advanced R Programming .
• Prior pharmaceutical experience and advanced knowledge of observational research study design and analytic methodologies
• Excellent analytic and communication skills with attention to detail
• Ability to effectively manage and prioritize multiple tasks and projects
  IQVIA is hiring to expand our dedicated Real-World Evidence (RWE) FSP team, working fully within the environment of a prominent pharmaceutical company. This senior data analyst role sits within our Data Science, Analytics, and Technology Solutions (DATS) team and will be responsible for leading the development of datasets and conducting longitudinal analyses for observational studies in the oncology therapeutic area under a single client portfolio., IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com
• IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.
• IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.