Senior RWE ExpertMake your mark for patients
About the role:
As a Senior RWE Expert, you will be responsible for designing and executing global real-world evidence (RWE) projects that:inform strategic internal decision-making thereby empowering differentiating R&D activities within UCBsupport external decision making by key stakeholder groups such as patients, regulators, policy makers, payers, and prescriberscontribute to the wider epidemiological and medical understanding of specific diseasesdevelop the underlying real world data infrastructure for a specific disease / disease area related to women of childbearing age (WoCBA) and other special patient populations (SPP), including elderly and pediatrics. You will drive the development of the overarching RWE Functional Strategic Plan for an asset in close collaboration with the Strategy lead for WoCBA/SPP.
What you'll do:
EXECUTION of RWE STUDIES on time and to budget:input to / help drive the Global RWE Strategy & Tactical WoCBA/SPP Plan based on request from the RWE Strategy Lead responsible for the respective patient population/assetE.g.: Epidemiology, Natural History/Burden, Care Pathways, Unmet Need; Gap analysis and new studies required for JCA; Background rates of safety outcomes; Regulatory studies including external control arms; Innovative hybrid study designs; Regulatory safety study commitments (PASS, PAES, PMS); Drug utilisation and early feedback post-launch; Comparative effectiveness including long term and patient centric outcomes; Data component of managed entry programmes / value-based contractswriting study concept; writing study protocol; developing SAP; meeting quality control and governance requirements, reporting against milestones; consultation to local study teams; mitigation for operational issues Leading Secondary Data Use Studies, including the most complex and high profile studies; and representing RWE on Primary Data Collection Study teams Collaborating with external vendors and medical experts on RWE projects, with BQS and RWE Analysts on the analysis plan Lead the interpretation of results and communicating results internally and externally Develop clearly defined evidence needs withthe Evidence Synthesis group for HE/HTA and value communication plans Safety / Pharmacovigilance teams for regulatory needs Supporting the RWE Strategy Lead to develop the overarching RWE Functional Strategic Plan for an asset Provide strategic input to internal stakeholders based on RWE activities and robust epidemiological and medical understanding of WoCBA/SPPIdentifying opportunities for innovative study designs, use of new data sources and advanced analytic techniques to solve complex evidence generation problems Consistently advocate for scientifically sound methods with internal and external stakeholders; being able to challenge and defend positions appropriately with a range of stakeholders Interested? For this position you'll need the following education, experience and skills:
Minimum Qualifications:- Master's Degree
- Experience successfully conceptualizing and delivering RWE projects using primary and secondary data (within the pharmaceutical industry or with a recognized expert consultancy or academic center of excellence)6 years of Global or regional experience
- Excellent and effective oral/written skills in English
Preferred Qualifications:- PhD in epidemiology or outcome research with additional depth and breadth of experience
- Ability to translate project work into scientific communications (e.g., abstracts, poster presentations, podium presentations, manuscripts)
- Combination of strong methodological quantitative knowledge, strategic, innovative thinking, and communication skills
- Experience in projects relating to fertility, preterm birth, obstetric illnesses, pregnancy, lactation and neonatal health AND/OR experience working with innovative RWE study designs and approaches
- Interested in incorporating advanced analytics, machine learning, and AI into traditional RWD approaches
- Background knowledge of industry trends and best practices, specifically related to epidemiology/outcomes research
- Subject matter expert with strong quantitative methods skills including training in the areas of epidemiology, pharmacoepidemiology, outcomes research, health economics, biostatistics, data science or related disciplines
- Ability to deliver impactful presentations to peers and/or internal stakeholders with a relaxed and proficient presentation style
- Experience successfully working with multidisciplinary cross functional and cross-cultural project teams
- Ability to use his/her relationships with internal and external stakeholder groups to provide strategic input through synthesized thinking, building advocacy and empowering implementation of the solutions in support of creating patient value and UCB portfolio performance
- Passion for maternal and infant health
Passion for innovation and creativity. Able to learn fast and adapt to new ways of working, be open-minded and science driven.
This positions reasonably anticipated base salary range is $164,000 to $215,300 per year. The actual salary offered will take into account internal equity and may also vary depending on the candidate's geographic region, job-related knowledge, skills, and experience, among other factors.
Are you ready to 'go beyond' to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!
About us:
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9,000 people in all four corners of the globe, inspired by patients and driven by science.
Why work with us?
At UCB, we don't just complete tasks, we create value. We aren't afraid to push forward, collaborate, and innovate to make our mark for patients. We have a caring, supportive culture where everyone feels included, respected, and has equal opportunities to do their best work. We 'go beyond' to create value for our patients, and always with a human focus, whether that's on our patients, our employees, or our planet. Working for us, you will discover a place where you can grow, and have the freedom to carve your own career path to achieve your full potential. At UCB, we've embraced a hybrid-first approach to work, bringing teams together in local hubs to foster collaborative curiosity. Unless explicitly stated in the description or precluded by the nature of the position, roles are hybrid with 40% of your time spent in the office. UCB is an equal opportunity employer. All employment decisions will be made without regard to any characteristic protected by applicable federal, state, or local law. UCB invites you to voluntarily self-identify during the application process. Provision of self-identification information is entirely voluntary and a decision to provide or not provide such information will not have any effect on your application for employment, your employment with UCB, or otherwise subject you to any adverse treatment. Any information you provide will be considered confidential and will be kept separate from your application and/or personnel file and will only be used in accordance with applicable laws, orders, and regulations. Should you require any adjustments to our process to assist you in demonstrating your strengths and capabilities contact us on US-Reasonable_Accommodation@ucb.com for application to US based roles. Please note should your enquiry not relate to adjustments; we will not be able to support you through this channel.
