Associate Director Real World Evidence Scientist (all genders) - (part-time/full-time)

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 s decision-marking.

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 epidemiology, public health), or quantitative data sciences, biostatisticsDoctoral and / or master’s degree (e.

g., PhD, MSc) in Epidemiology, Public Health or related fieldStrong experience in RWE / D within the pharmaceutical industry, particularly in the application of RWE in drug development for rare indicationsDemonstrable experience in leading RWE generation plans and studies end-to end, including application of innovative designs and methodsExcellent oral and written communication skills and demonstrated ability to engage and communicate scientific evidence to peers and at scientific meetingsCollaborative, proactive working style, with ability to work independently.