Senior Associate, Real World Data (RWD) Analyst (EMEA)

Posted 4 Days Ago
Be an Early Applicant
Hiring Remotely in Warsaw, Warszawa, Mazowieckie, POL
In-Office or Remote
Senior level
Biotech
The Role
Supports real-world evidence services by programming analyses of observational, claims, hospital, EHR, and registry data. Develops analysis-ready datasets, tables, figures, listings, validation programs, and documentation according to analytic plans. Performs quality checks, resolves discrepancies, communicates project status, follows SOPs, improves analytic processes, and guides junior analysts. The role also contributes to team knowledge-sharing and repeat business through high-quality client deliverables.
Summary Generated by Built In

Job Overview:

The Senior Associate, Real World Data (RWD) Analyst, in our Fortrea Consulting group, is responsible for supporting our Real-world Evidence (RWE) services through successful delivery of complex analyses of data generated from global prospective and retrospective observational studies or existing secondary data sources (e.g., claims, hospital administration, electronic health records, registries). The Senior Associate, RWD Analyst follows analytic plans for data presentation under the guidance of our RWE biostatisticians and epidemiologists.

Summary of Responsibilities:

Client Delivery

  • Provide programming for the analysis of RWD from diverse sources including observational studies and existing secondary data sources (e.g., claims, hospital administration, electronic health records, registries)
  • Develop analysis-ready datasets from source data, including derivation of analytic variables, following an analytic plan
  • Independently develop tables/figures/listings (TFLs) from analytic datasets and following an analytic plan
  • Provide programs to validate analysis datasets and results presented in TFLs and resolve discrepancies with minimal oversight
  • Create and maintain documentation of programming for assigned deliverables
  • Provide quality cross-checks of written deliverables to analytic results
  • Communicate accurate and timely status updates to RWE biostatisticians, epidemiologists, and team members
  • Provide analytic programming of other data sources for various projects, as needed

Process Improvement

  • Follow standard operating procedures (SOPs) relevant to assigned projects
  • Identify opportunities to enhance productivity, quality, and efficiency in analytic processes

People

  • Provide informal guidance to Associate, RWD Analysts
  • Participate in department meetings to share knowledge and insights
  • Maintain a standard of personal behavior and business ethics in line with Fortrea culture

Business Development

  • Contribute to repeat business through delivery of quality analyses and deliverables
  • And all other duties as needed or assigned

Qualifications (Minimum Required):

  • Bachelor’s degree in statistics, mathematics, epidemiology, or another relevant field
  • Fortrea may consider relevant and equivalent experience and successful project outcomes in lieu of educational requirements
  • Proficiency in relevant programming language that meets current client demand (e.g., SAS, R, Python)
  • Proficiency in SAS macro language
  • Working knowledge of Microsoft Word, PowerPoint, and Excel
  • Ability to solve problems independently
  • Ability to follow defined processes
  • Strong attention to detail
  • Strong oral and written communication
  • Team player mentality

Experience (Minimum Required):  

  • ≥3 years of health research data analysis experience

Preferred Qualifications:

  • Bachelor’s degree or higher with a strong focus in statistics
  • Experience conducting analyses of observational study data
  • Proficiency in CDISC standards (e.g., writing SDTM and ADaM specifications)
  • Experience applying CDISC standards to observational study data
  • Analytic experience with existing secondary data sources (e.g., claims, hospital administration, electronic health records, registries)
  • Ability to challenge conventional thinking to develop solutions

Physical Demands / Work Environment:

  • Home-based environment
  • Varied hours may be required
  • On occasion, must be able to work in the evenings and on weekends to meet project deadlines
  • Ability to work in an upright and/or stationary position for 6-8 hours per day
  • Repetitive hand movement of both hands with the ability to make fast, simple, repeated movements of the fingers, hands, and wrists to operate lab equipment
  • Occasional crouching, stooping, with frequent bending and twisting of upper body and neck
  • Ability to access and use a variety of computer software developed both in-house and off-the-shelf
  • Light to moderate lifting and carrying, or moving of objects, including luggage and laptop computer with a maximum lift of 15-20 lbs
  • Regular and consistent attendance

Learn more about our EEO & Accommodations request here.

Skills Required

  • Bachelor's degree in statistics, mathematics, epidemiology, or another relevant field
  • Relevant and equivalent experience and successful project outcomes may substitute for educational requirements
  • Proficiency in a relevant programming language, such as SAS, R, or Python
  • Proficiency in SAS macro language
  • Working knowledge of Microsoft Word, PowerPoint, and Excel
  • At least 3 years of health research data analysis experience
  • Ability to solve problems independently
  • Ability to follow defined processes
  • Strong attention to detail
  • Strong oral and written communication skills
  • Team player mentality
  • Bachelor's degree or higher with a strong focus in statistics
  • Experience analyzing observational study data
  • Proficiency in CDISC standards, including SDTM and ADaM specifications
  • Experience applying CDISC standards to observational study data
  • Experience analyzing claims, hospital administration, electronic health records, or registry data
  • Ability to challenge conventional thinking to develop solutions
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The Company
HQ: Durham, NC
10,811 Employees

What We Do

Fortrea (Nasdaq: FTRE) is a leading global provider of clinical development and patient access solutions to the life sciences industry. We partner with emerging and large biopharmaceutical, medical device and diagnostic companies to drive healthcare innovation that accelerates life changing therapies to patients in need. Fortrea provides phase I-IV clinical trial management, clinical pharmacology, differentiated technology-enabled trial solutions and post-approval services. Fortrea’s solutions leverage three decades of experience spanning more than 20 therapeutic areas, a passion for scientific rigor, exceptional insights and a strong investigator site network. Our talented and diverse team working in more than 90 countries is scaled to deliver focused and agile solutions to customers globally. Learn more about how Fortrea is becoming a transformative force from pipeline to patient at Fortrea.com.

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