Data Scientist as RWE Manager - Clinical Trials, Evidence Synthesis (f/m/d)

ZipRecruiter; Heidenheim an der Brenz; Vor Ort; EUR 70.000 - 90.000; Vollzeit

Zusammenfassung

A leading company in medtech is seeking a highly skilled RWD/RWE Manager to join its Evidence Department. This role involves developing strategies for real-world data to support regulatory and market access efforts. Ideal candidates will have 3+ years of related experience, proficiency in statistical programming, and strong project management skills. Enjoy flexible working conditions, attractive leave options, and a comprehensive benefits package.

Leistungen

Flexible working conditions

International mobile working opportunities

Childcare subsidy

30 days paid leave per year

Company pension plan

Access to fitness and wellness studios

Job Bike Leasing and discounts

Qualifikationen

• 3+ years of experience in generating RWD and RWE in medtech or healthcare.
• Proven experience with real-world data sources like EHRs and claims.
• Strong knowledge of real-world study designs and global regulatory requirements.

Aufgaben

• Design and implement RWD and RWE strategies for clinical evidence.
• Lead data extraction and analysis from diverse RWD sources.
• Communicate RWE findings through reports and presentations.

Kenntnisse

Statistical programming

Data analysis

Project management

Communication

Health economics

Ausbildung

Advanced degree in epidemiology, biostatistics, health economics, public health, data science

Tools

SAS

R

Python

Jobbeschreibung

Job Description

At HARTMANN, we're all in to help, care, protect and grow. We support healthcare professionals so they can focus on what really matters: positively impacting people's lives. We develop solutions that make a difference. With your commitment, you can grow in your role every day. At HARTMANN, we believe in the difference you can make.

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 Evidence Department. The successful candidate will lead the development and execution of RWD and RWE strategies to support clinical, regulatory, and market access efforts for our medtech products. This role is crucial 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 the Evidence Department (Clinical Trials, Evidence Synthesis, Health Economics, Diagnostic/Prognostic Research) and beyond, including regulatory, clinical, 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, 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 RWD and 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 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 hours and mobile working
• International mobile working opportunities
• Attractive work-life balance options, including childcare subsidy
• 30 days paid leave per year, plus special leave for life events, vacation pay, and annual bonus
• Company pension plan with employer contributions and deferred compensation options
• Facilities include parking, canteen with café bar, and employee shop offers
• Access to over 6000 fitness and wellness studios (EGYM Wellpass)
• Various health initiatives like screenings, online mental health courses, massages, yoga, etc.
• Job Bike Leasing and discounts on travel, fashion, and technology via our benefits platform