Associate Director RWE N&I (all genders) - part-time possible

TN Germany; Darmstadt; Vor Ort; EUR 80.000 - 100.000; Teilzeit

Zusammenfassung

Ein innovatives Unternehmen sucht einen Associate Director für Real-World Evidence, der die Strategie und Umsetzung von RWE-Studien leitet. In dieser Schlüsselrolle werden Sie die wissenschaftliche Führung übernehmen und die Integration von realen Daten in Entscheidungsprozesse unterstützen. Ihr Beitrag wird entscheidend sein, um die Entwicklung von Medikamenten zu beschleunigen und sicherzustellen, dass evidenzbasierte Lösungen schnell verfügbar sind. Wenn Sie eine Leidenschaft für Datenanalyse und interdisziplinäre Zusammenarbeit haben, ist dies die perfekte Gelegenheit für Sie.

Qualifikationen

• Hintergrund in Gesundheits- und Lebenswissenschaften oder quantitativen Datenwissenschaften.
• Erfahrung in der pharmazeutischen Industrie und RWE-Studien.

Aufgaben

• Leiten der RWE-Strategie und -Studien über den Lebenszyklus von Medikamenten.
• Gestaltung und Umsetzung von nicht-interventionellen Studien.

Kenntnisse

Epidemiologie

Biostatistik

Datenanalyse

Kommunikationsfähigkeiten

Ausbildung

PhD in Epidemiologie

MSc in Public Health

Jobbeschreibung

Associate Director RWE N&I (all genders) - part-time possible, Darmstadt

Client:

Location:

Job Category:

Other

EU work permit required:

Yes

Job Reference:

55699ae7ccd6

Job Views:

2

Posted:

09.05.2025

Expiry Date:

23.06.2025

Job Description:

An exciting opportunity awaits you within the Patient Focused Real World Evidence (PRWE) Team. As passionate leaders of patient focused real world data, evidence generation, and epidemiology, we are uniquely placed to enable fit-for-purpose visionary solutions with real world and patient focused data from early development and throughout the drug life span. Our team operates with a proactive and agile approach, as a trusted partner in qualitative and quantitative sciences, all while striving towards the common goal to deliver more medicines to more patients faster.

As a key member of our team, you will drive the Real-World Evidence and Data (RWE/D) strategy and studies across the lifecycle of drugs, with a particular focus on drug development and excellence in integrated evidence planning. You will provide scientific leadership and expertise to ensure that fit-for-purpose RWD are integrated in evidence generation plans and available in a timely manner to support regulatory submissions and program decision-making.

You will lead the design, implementation, and oversight of disease or drug-specific Non-Interventional (NIS) / RWE studies, encompassing safety-related studies, external control arm studies, and regulatory-grade studies. Your work will involve inspiring cross-functional collaboration, in a unique partnership with other quantitative scientists while maintaining and expanding our external collaborations.

Who you are:

• Preferably a background in health and life sciences (MD, pharmacist, epidemiologist, public health), or quantitative data sciences, biostatistics
• Doctoral and/or master's degree (e.g., PhD, MSc) in Epidemiology, Public Health, or related field
• Strong experience in RWE/D within the pharmaceutical industry, particularly in the application of RWE in drug development for rare indications
• Demonstrable experience in leading RWE generation plans and studies end-to-end, including application of innovative designs and methods
• Excellent oral and written communication skills and demonstrated ability to engage and communicate scientific evidence to peers and at scientific meetings
• Collaborative, proactive working style, with ability to work independently