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Data Analyst - Registries/Epidemiology

Pharmaceutical Product Development (PPD)

SE-Stockholm

The Team

Evidera has been providingepidemiology, data analytics, andoutcomes research services to clients in the biopharmaceutical industry for over 19 years.The Real-World Evidence team supportspharmaceutical,biotechnologyandmedical devicecompanies in thedesign and conduct of epidemiology studiesthroughout the product lifecycle, from early pre-launch planning to launch and post-marketing management. Our focus is on helping our clientsidentify evidence gaps and rapidlybuildepidemiologic andeconomic evidence to demonstrateeffectiveness and safetyand support the value of their products. Through analysis oflargeexistinghealth databases(e.g., medical claims, electronic health records, registries, etc.), we provide key information such as: The incidence and prevalence of diseases and co-morbidities Theidentification andimpact of risk factorson disease outcomes Burden of diseaseand identification of unmet needs Treatment patterns,drug utilization,medicationadherence Comparative effectiveness Comparative safety Resource utilization

We use epidemiologic methods to build knowledge ofthe relationships between patient, drug, clinical and disease factorsthatsignificantly aidsourclientsand the patients they serveinunderstanding health conditions andnavigating potential drug-event causal relationships as well as in building stronger evidence-based value messages.

Position Overview

We are looking for aData Analyst IIIin Stockholm, with the aim toimplement a broad range ofdatamanagementandstatisticalanalysesusing data from the Scandinavian Registries. In this mid-level role, it is expected candidates willwork independently,andwill be able providesubstantivesupport to the projectteamintheplanning and design phases of a project.In addition, the Data Analyst III will be involved in developing the ethics and data application to the relevant authoritiesin order toaccess the data.

In particular, theData Analyst III will: Implements or oversees implementation of cohort selection, variable derivation,anddatamanagement to convert the raw data filesinto analytical datasets Programs tablesof resultsfollowing the Statistical Analyses Plan (SAP) developed by the project team Reviews and provides critical input into SAPs, study reports, and other relevant documentation for internal or external communication Develops the ethics and data applications forScandinavian registrydata access Teaches/mentors junior staff, Participates in thevalidation and review of others' programs Presents to internal teams and suggests alternative approaches towards analyses, documentation, and general process improvements Supports as needed other programmers in the analyses of data from other existing databases in Europe and the United States

The Team

Evidera has been providingepidemiology, data analytics, andoutcomes research services to clients in the biopharmaceutical industry for over 19 years.The Real-World Evidence team supportspharmaceutical,biotechnologyandmedical devicecompanies in thedesign and conduct of epidemiology studiesthroughout the product lifecycle, from early pre-launch planning to launch and post-marketing management. Our focus is on helping our clientsidentify evidence gaps and rapidlybuildepidemiologic andeconomic evidence to demonstrateeffectiveness and safetyand support the value of their products. Through analysis oflargeexistinghealth databases(e.g., medical claims, electronic health records, registries, etc.), we provide key information such as: The incidence and prevalence of diseases and co-morbidities Theidentification andimpact of risk factorson disease outcomes Burden of diseaseand identification of unmet needs Treatment patterns,drug utilization,medicationadherence Comparative effectiveness Comparative safety Resource utilization

We use epidemiologic methods to build knowledge ofthe relationships between patient, drug, clinical and disease factorsthatsignificantly aidsourclientsand the patients they serveinunderstanding health conditions andnavigating potential drug-event causal relationships as well as in building stronger evidence-based value messages.

Position Overview

We are looking for aData Analyst IIIin Stockholm, with the aim toimplement a broad range ofdatamanagementandstatisticalanalysesusing data from the Scandinavian Registries. In this mid-level role, it is expected candidates willwork independently,andwill be able providesubstantivesupport to the projectteamintheplanning and design phases of a project.In addition, the Data Analyst III will be involved in developing the ethics and data application to the relevant authoritiesin order toaccess the data.

In particular, theData Analyst III will: Implements or oversees implementation of cohort selection, variable derivation,anddatamanagement to convert the raw data filesinto analytical datasets Programs tablesof resultsfollowing the Statistical Analyses Plan (SAP) developed by the project team Reviews and provides critical input into SAPs, study reports, and other relevant documentation for internal or external communication Develops the ethics and data applications forScandinavian registrydata access Teaches/mentors junior staff, Participates in thevalidation and review of others' programs Presents to internal teams and suggests alternative approaches towards analyses, documentation, and general process improvements Supports as needed other programmers in the analyses of data from other existing databases in Europe and the United States

Education, Professional Skills & Experience Bachelors plus 5 years of experience in the health industry / consulting environment, or Masters plus 3 years of experience in the health industry / consulting environment, or Doctorate plus 2 years of experience in the health industry / consulting environment. Advanced knowledge of SAS Base, Microsoft Excel, Word, PowerPoint, Access and Outlook essential Knowledge of SAS macro will be an advantage Intermediate understanding of epidemiology, pharmacoepidemiology, or biostatistics. Fluent in English and Swedish Experience using data from Denmark, Norway, Sweden or Finlandrequired Basic experiencein survival analyses, regression models and propensity score development desired.

Personal Skills & Competencies

•Inquisitive, curious, passionate about data, attention to minute details.

•Communicates and documents 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.

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

•Presents ideas to individuals and groups in a formal presentation setting.

•Analyzes, responds to, and resolves enquiries, issues and escalations.

•Evaluates, plans and accomplishes multiple work goals in a timely fashion.

•Ability 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 in the consulting environment.

•Desire and ability to guide and coach junior levels of scientific staff.

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.

Perks:

We offer a competitive salary and benefits package, with clear opportunities for growth and careerprogression.You will have the opportunity to work on multiple projects with some of the industry’s leading researchers. Ouroffices boasta fun and collaborative working environment, frequent socialeventsand a robust support system. We are committed to providing training and professional development, with ample opportunity to advance, forallour staff.

Evidera’s Core Competencies: Customer Focus Initiative Teamwork Problem Solving/Judgment Accountability

If you resonate with our core competencies and want to contribute to research and consulting services driven by world-class science and thought leadership, then please submit your application – we’d love to hear from you.

Evidera, Inc. provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, sex, national origin, age, genetics, sexual orientation, gender preference,disability, or status as a qualified individual with a disability or protected veteran.

Education, Professional Skills & Experience Bachelors plus 5 years of experience in the health industry / consulting environment, or Masters plus 3 years of experience in the health industry / consulting environment, or Doctorate plus 2 years of experience in the health industry / consulting environment. Advanced knowledge of SAS Base, Microsoft Excel, Word, PowerPoint, Access and Outlook essential Knowledge of SAS macro will be an advantage Intermediate understanding of epidemiology, pharmacoepidemiology, or biostatistics. Fluent in English and Swedish Experience using data from Denmark, Norway, Sweden or Finlandrequired Basic experiencein survival analyses, regression models and propensity score development desired.

Personal Skills & Competencies

•Inquisitive, curious, passionate about data, attention to minute details.

•Communicates and documents 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.

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

•Presents ideas to individuals and groups in a formal presentation setting.

•Analyzes, responds to, and resolves enquiries, issues and escalations.

•Evaluates, plans and accomplishes multiple work goals in a timely fashion.

•Ability 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 in the consulting environment.

•Desire and ability to guide and coach junior levels of scientific staff.

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.

Perks:

We offer a competitive salary and benefits package, with clear opportunities for growth and careerprogression.You will have the opportunity to work on multiple projects with some of the industry’s leading researchers. Ouroffices boasta fun and collaborative working environment, frequent socialeventsand a robust support system. We are committed to providing training and professional development, with ample opportunity to advance, forallour staff.

Evidera’s Core Competencies: Customer Focus Initiative Teamwork Problem Solving/Judgment Accountability

If you resonate with our core competencies and want to contribute to research and consulting services driven by world-class science and thought leadership, then please submit your application – we’d love to hear from you.

Evidera, Inc. provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, sex, national origin, age, genetics, sexual orientation, gender preference,disability, or status as a qualified individual with a disability or protected veteran.

Job posted: 2021-01-20

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