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RWD/RWE Manager(m/w/x)

HARTMANN
Heidenheim an der Brenz

You lead the development and implementation of real-world data strategies, collaborating with various teams to generate evidence and ensure compliance while effectively communicating findings to stakeholders.

Anforderungen

  • •Advanced degree in epidemiology or related fields
  • •3+ years of experience in real-world data
  • •Proven experience with real-world data sources
  • •Hands-on experience with causal inference methods
  • •Proficiency in statistical programming tools
  • •Strong knowledge of real-world study designs
  • •Expertise in GDPR and data privacy laws
  • •Strong project management and communication skills

Deine Aufgaben

  • •Design and implement RWD and RWE strategies.
  • •Collaborate with cross-functional teams for evidence generation.
  • •Develop study protocols for observational studies and registries.
  • •Lead data extraction, cleaning, and analysis from diverse sources.
  • •Communicate RWE findings through reports and presentations.
  • •Ensure compliance with regulatory guidelines and data privacy.
  • •Stay updated on trends in real-world data and evidence generation.

Deine Vorteile

Flexible working conditions
International mobile working
Childcare subsidy
30 days paid leave
Company pension plan
Plenty of parking spaces
Access to fitness studios
Various health and fitness offers
Job bike leasing
Attractive discounts

Original Beschreibung

## Helps. Cares. Protects. Join our team as **RWD/RWE Manager (f/m/d)** DEU-Heidenheim We are seeking a highly skilled and motivated Real-World Data (RWD) / Real-World Evidence (RWE) Manager to join our dynamic team (Evidence Generation Department). The successful candidate will lead the development and execution of RWD and RWE strategies to support the clinical, regulatory, and market access efforts of our medtech products. This role is critical in translating real-world insights into evidence that informs healthcare decisions and accelerates the adoption of innovative medical technologies. Currently we are conducting several RWD comparative effectiveness studies using data from the EU/UK and the US. **Responsibilities:** * Design and implement **RWD** and **RWE** **strategies** to generate clinical, safety, and economic evidence for medtech products * Collaborate with **cross-functional teams** within Evidence Generation Department (Clinical Trials, Evidence Synthesis, Health Economics, and Diagnostic/Prognostic Research), and beyond, including regulatory, clinical affairs, market access, marketing, and sales to integrate RWE into product development and lifecycle management * Develop **study protocols**, including observational studies, registries, and post-market surveillance, to gather and analyze real-world data * Lead data extraction, cleaning, analysis, and interpretation from diverse real-world data sources such as electronic health records (**EHR**), claims data, patient registries, and wearables * Communicate **RWE findings** through reports, scientific publications, white papers, and presentations to internal stakeholders, regulatory authorities, and external audiences * Ensure **compliance** with applicable regulatory guidelines and industry standards for data privacy, security, and ethical use of patient data * Stay up to date with **emerging trends** and **technologies** in real-world data and evidence generation, and apply innovative methods to optimize RWD and RWE strategies **Qualifications:** * Advanced degree in epidemiology, biostatistics, health economics, public health, data science, or related fields * 3+ years of experience in generating real-world data (RWD) and evidence (RWE), preferably in medtech, pharma, or healthcare * Proven experience with real-world data sources (EHR, claims, registry data) and RWE studies for regulatory or HTA purposes * Experience working with different types of RWD and hands-on experience with causal inference methods * Proficiency in statistical programming and data analysis tools (SAS, R, Python) and familiarity with RWD platforms (e.g., Flatiron, IQVIA) * Strong knowledge of real-world study designs (retrospective cohort, case-control, registry-based) and global regulatory requirements (FDA, EMA) * Expertise in GDPR, data privacy laws, and health economic models with evidence synthesis * Strong project management, communication skills, and experience in medtech or digital health solutions **Benefits:** * Flexible working conditions, such as flexible working hours and mobile working * International Mobile Working * Attractive ways of combining work and family life, e.g. childcare subsidy * 30 days paid leave per year, plus special leave for exceptional life events as well as vacation pay and special annual payment according to collective agreement * Company pension plan with attractive employer contribution incl. matching model for deferred compensation * Plenty of parking spaces, canteen with café bar and ongoing offers in the employee shop * Access to over 6000 fitness and yoga studios, swimming pools as well as Crossfit and bouldering halls (EGYM Wellpass) * Various health and fitness offers, e.g. skin cancer screenings, online courses for mental health, massage offers, yoga during lunch break etc. * Job Bike Leasing * Attractive discounts on e.g. travel, fashion and technology via our corporate benefits platform​ Your personal contact: **​Sophia Zoller** *\*the male form is for simplification only and stands for the gender-neutral description of the profession* # RWD/RWE Manager (f/m/d)
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