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

TN United Kingdom; Greater London; On-site; GBP 60,000 - 100,000; Full time

Job summary

An exciting opportunity awaits you as a key member of a dynamic team focused on Real World Evidence in Oncology. This role offers the chance to lead innovative studies that integrate real-world data into drug development, ensuring that critical evidence supports decision-making and regulatory submissions. You will collaborate with cross-functional teams and external partners, driving forward the mission to deliver more effective treatments to patients. If you are passionate about making a significant impact in the pharmaceutical industry and have a strong background in health sciences, this position is perfect for you.

Qualifications

• Background in health/life sciences or quantitative data sciences.
• Strong experience in RWE/D within the pharmaceutical industry.

Responsibilities

• Drive Real-World Evidence strategy and studies for drug development.
• Lead design and oversight of disease-specific RWE studies.

Skills

Leadership

Communication Skills

Collaboration

Epidemiology

Biostatistics

Data Analysis

Education

Doctoral degree in Epidemiology

Master’s degree in Public Health

Job description

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Director Real World Evidence (Oncology) all genders/part-time/full-time, Feltham

Location: Feltham, United Kingdom

Job Category:

Other

EU work permit required:

Yes

Job Reference:

2f42973251a5

Job Views:

2

Posted:

18.04.2025

Expiry Date:

02.06.2025

Job Description:

An exciting opportunity awaits you within the Patient Focused Real World Evidence (PRWE) Team for Oncology (Early Phase Development). As passionate leaders of patient focused real world data, evidence generation, and epidemiology, we are uniquely placed to enable fit-for-purpose visionary solutions. 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, with a particular focus on early drug development and 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 to support program's decision-making and regulatory submissions.

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

Who you are:

1. Background in health and life sciences (epidemiology, public health, MD, pharm D), or quantitative data sciences, biostatistics.
2. Doctoral and/or master’s degree (e.g., PhD, MSc) in Epidemiology, Public Health or related field.
3. Strong experience in RWE/D within the pharmaceutical industry, particularly in the application of RWE in drug development for rare indications and early phase development.
4. Prior experience in supporting the therapeutic area of Oncology.
5. Demonstrable experience in leading RWE generation plans and studies end-to-end, including application of innovative designs and methods.
6. Excellent oral and written communication skills and demonstrated ability to engage and communicate scientific evidence to peers and at scientific meetings.
7. Collaborative, proactive working style, with ability to work independently.