Data Analyst II – Real World Evidence

Pharmaceutical Product Development (PPD)

SE-Stockholm-Stockholm SE Sundbyberg


The Team

The Real-World Evidence team supports biopharmaceutical companies throughout the product lifecycle, from early pre-launch planning to launch and post-marketing management. Our focus is on helping our clients in the pharmaceutical/ biotechnology/ medical device industries build economic and epidemiological evidence to demonstrate and support the value of their products. Through analysis of individual patient databases (e.g., medical claims, electronic health records, registries, etc.), we may provide key information such as:

Treatment patterns and drug utilization

Resource utilization

The incidence and prevalence of diseases and co-morbidities

The incidence of adverse events

The impact of various risk factors

Cost-effectiveness

Burden of disease

Comparative effectiveness data

Position Overview

The Data Analyst will be responsible for implementing a range of simple to moderate analyses in support of epidemiologic studies for a key client account. This individual will work independently to support the sponsor team on epidemiological studies using large health administrative databases such as MarketScan/Truven, Optum, CPRD, etc. This individual will also be required to provide input in the planning and designing phases of projects under the supervision of a more senior staff member.The main programming language is SAS (e.g., SAS Base, SAS Stat, SAS Macro), but this position also requires knowledge of Python, PySpark or R. Promising SAS candidates without these additional skills will be provided the opportunity for additional training. In addition, this individual will participate in quantitative analysis of retrospective and prospective data, clinical and observational, and both existing data and data collected explicitly for research objectives (de novo data collection) working with the researchers in Evidera.

Role Responsibilities:

Implements routine data management tasks to convert raw data files into analytical datasets

Performs descriptive and survival analyses independently and moderately advanced statistical analyses working under supervision of a more senior staff.

Ability to provide thoughtful input into a protocol or statistical analyses plan with increasing involvement and responsibility for planning and design phases of projects.

Writes, modifies and maintains programs to perform data management and analyses, under the guidelines of Real-World Evidence team’s good programming practices.

Conducts validation and review of programs developed by other programmers in the team.

Handles client interactions to discuss protocol content and present study results

The Team

The Real-World Evidence team supports biopharmaceutical companies throughout the product lifecycle, from early pre-launch planning to launch and post-marketing management. Our focus is on helping our clients in the pharmaceutical/ biotechnology/ medical device industries build economic and epidemiological evidence to demonstrate and support the value of their products. Through analysis of individual patient databases (e.g., medical claims, electronic health records, registries, etc.), we may provide key information such as:

Treatment patterns and drug utilization

Resource utilization

The incidence and prevalence of diseases and co-morbidities

The incidence of adverse events

The impact of various risk factors

Cost-effectiveness

Burden of disease

Comparative effectiveness data

Position Overview

The Data Analyst will be responsible for implementing a range of simple to moderate analyses in support of epidemiologic studies for a key client account. This individual will work independently to support the sponsor team on epidemiological studies using large health administrative databases such as MarketScan/Truven, Optum, CPRD, etc. This individual will also be required to provide input in the planning and designing phases of projects under the supervision of a more senior staff member.The main programming language is SAS (e.g., SAS Base, SAS Stat, SAS Macro), but this position also requires knowledge of Python, PySpark or R. Promising SAS candidates without these additional skills will be provided the opportunity for additional training. In addition, this individual will participate in quantitative analysis of retrospective and prospective data, clinical and observational, and both existing data and data collected explicitly for research objectives (de novo data collection) working with the researchers in Evidera.

Role Responsibilities:

Implements routine data management tasks to convert raw data files into analytical datasets

Performs descriptive and survival analyses independently and moderately advanced statistical analyses working under supervision of a more senior staff.

Ability to provide thoughtful input into a protocol or statistical analyses plan with increasing involvement and responsibility for planning and design phases of projects.

Writes, modifies and maintains programs to perform data management and analyses, under the guidelines of Real-World Evidence team’s good programming practices.

Conducts validation and review of programs developed by other programmers in the team.

Handles client interactions to discuss protocol content and present study results

Education fields: Epidemiology, Health Economics, Biostatistics or related field

PhD with at some relevant work experience; MSc with at least 2 years of relevant work experience, or BSc with significant work experience in a similar industry/ consulting environment.

Demonstrated experience in quantitative methods in health economics, health services research, epidemiology or statistics with the focus on data analysis using observational retrospective data, claims data, or clinical trial data using SAS (e.g., SAS Base, SAS Stat, SAS Macro)

Working experience in Python, PySpark or R; SQL also relevant. Training will be provided for promising candidates without these additional experiences.

Experience working with large databases such as MarketScan/Truven, Flatiron/EMR data, or similar

Knowledge of scientific research methods and practical knowledge of research implementation.

Knowledge of fundamentals of health economics and epidemiology.

Knowledge of relevant methodology and statistics.

Experience in Excel, MS Word, PowerPoint, Access and Outlook.

Personal Skills & Competencies

Demonstrated ability to communicate and document information effectively in written English, including the ability to produce reports, documents, emails and other written pieces which are well-organized, free from errors, and are appropriately adjusted to the characteristics and needs of the audience.

Strong organizational, time-management, prioritization and decision-making skills necessary to evaluate, plan and accomplish multiple work goals in a timely fashion.

Able to quickly learn and apply new information, skills and procedures.

Proactive and positive approach to tasks and projects, as well as resilience when encountering process, project, budget or client changes that are inherent to the consulting environment.

Solid communication and interpersonal skills including the ability to quickly develop and sustain positive rapport with internal and external contacts in person, over the phone and by email.

Experience presenting ideas to individuals and groups in a formal presentation setting.

Able to analyze complex issues and evidence, identify cause-effect relationships, and generate effective solutions.

About Evidera:

Evidera is a business within in Pharmaceutical Product Development, LLC (PPD) a leading global contract research organization (CRO), and a is a preeminent provider of evidence-based solutions. We provide integrated scientific expertise and global operational capabilities to help clients generate the evidence needed to optimize the market access and commercial potential of products.

Education fields: Epidemiology, Health Economics, Biostatistics or related field

PhD with at some relevant work experience; MSc with at least 2 years of relevant work experience, or BSc with significant work experience in a similar industry/ consulting environment.

Demonstrated experience in quantitative methods in health economics, health services research, epidemiology or statistics with the focus on data analysis using observational retrospective data, claims data, or clinical trial data using SAS (e.g., SAS Base, SAS Stat, SAS Macro)

Working experience in Python, PySpark or R; SQL also relevant. Training will be provided for promising candidates without these additional experiences.

Experience working with large databases such as MarketScan/Truven, Flatiron/EMR data, or similar

Knowledge of scientific research methods and practical knowledge of research implementation.

Knowledge of fundamentals of health economics and epidemiology.

Knowledge of relevant methodology and statistics.

Experience in Excel, MS Word, PowerPoint, Access and Outlook.

Personal Skills & Competencies

Demonstrated ability to communicate and document information effectively in written English, including the ability to produce reports, documents, emails and other written pieces which are well-organized, free from errors, and are appropriately adjusted to the characteristics and needs of the audience.

Strong organizational, time-management, prioritization and decision-making skills necessary to evaluate, plan and accomplish multiple work goals in a timely fashion.

Able to quickly learn and apply new information, skills and procedures.

Proactive and positive approach to tasks and projects, as well as resilience when encountering process, project, budget or client changes that are inherent to the consulting environment.

Solid communication and interpersonal skills including the ability to quickly develop and sustain positive rapport with internal and external contacts in person, over the phone and by email.

Experience presenting ideas to individuals and groups in a formal presentation setting.

Able to analyze complex issues and evidence, identify cause-effect relationships, and generate effective solutions.

About Evidera:

Evidera is a business within in Pharmaceutical Product Development, LLC (PPD) a leading global contract research organization (CRO), and a is a preeminent provider of evidence-based solutions. We provide integrated scientific expertise and global operational capabilities to help clients generate the evidence needed to optimize the market access and commercial potential of products.


2020-08-03 00:00:00


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