Real World Evidence Scientists (Belgium, UK, USA, Germany)
February 28, 2018
Full Time - Experienced
Health Care Safety/Epidemiology, Health Economics/Outcomes Research
Help us transform patients’ lives
At UCB, we put heart, soul and skills into making a difference for people living with severe disease. Working together to push the boundaries, we blend the best of our talents to unlock innovation. We believe that one day, Real World Data (RWD) will be the most influential source of evidence in healthcare, ensuring every patient gets the right care. Will you join us in our pioneering adventure?
We are looking to fill 3 positions of Real World Evidence (RWE) Scientists (neurology, bone, inflammation) to strengthen our global Real-World Evidence (RWE) Practice team, which is comprised of epidemiologists, analysts, methodologists, and health outcomes experts. The positions will be based in one of our global locations (Brussels, Belgium, Slough, UK, Monheim, Germany, or Raleigh, North Carolina, USA). The RWE Practice strives to harness the full potential real-world data to support UCB’s mission to enhance our understanding of disease and the real-life experiences of patients so that UCB can deliver the right drug and the right care to the right patient.
As a RWE Scientist, you will be responsible for designing and executing projects using real-world data to:
support external decision making by key stakeholder groups such as policy makers, payers, and prescribers
contribute to the wider epidemiological and medical understanding of specific diseases
Furthermore, as a RWE Scientist you will contribute by:
Co-creating Global RWE Strategy & Tactical Plan with RWE disease area Leads
Leading RWE study execution, including study design and analysis specification and protocol development
Liaising with RWE Methodologists concerning study design and RWD Specialist concerning choice of data source on an as needed basis
Managing RWE contractors and overseeing their execution of systematic and pragmatic literature reviews, analytical projects, and report creation
Providing RWE Analysts with clarifications concerning protocol implementation
Driving interpretation of analysis in collaboration with RWE Lead Scientist & internal stakeholders, and communicating analysis interpretation internally and externally
Co-creating RWE publication plan with RWE Lead Scientist and managing internal & external communication including scientific publications
For this position, you’ll need the following education, experience and skills:
Minimally required experience: 3 years successfully delivering global and/or local RWE projects (studies using large healthcare databases, prospective observational studies, epidemiology support of drug safety…) from conceptualisation to publication within the pharmaceutical industry or with a recognised expert consultancy or academic centre of excellence; demonstrable publication record in relevant peer reviewed scientific and/or clinical journals
Desirable/preferred experience: as above; depth and breadth of experience will be reflected in the grade
Training in the areas of epidemiology, pharmacoepidemiology, outcomes research, health economics, biostatistics, data science or related fieldsGood background knowledge of industry trends and best practices, specifically related to epidemiology/outcomes research
Good knowledge and understanding of applicable regulations in pharmacovigilance and clinical development
Ability to solve scientific and technical questions/problems related to the epidemiology and pharmacovigilance environment
Expertise in the EU5/ US healthcare environment (and changes therein)
Ability to leverage changes in healthcare systems to help plan and drive development of innovative patient access solutions in support of UCB compounds, resulting in value for institutional/individual stakeholders in addition to patients and physicians
Excellent and effective oral/written skills in English
Able to deliver presentations to senior management or industry audiences with a relaxed and proficient presentation style
Ability to develop and maintain strong collaborative relationships with key partners and stakeholders
Experience successfully working with multidisciplinary cross functional and cross-cultural project teams
Ability to proactively use his/her relationships with internal and external stakeholder groups to synthesize thinking, build advocacy and empower implementation of the solutions in support of UCB portfolio performance and patient outcome
Drive for innovation and creativity
Visionary, strategic and tactical capabilities
Internal Number: 53061
UCB is a global biopharmaceutical company, with a focus on neurology and immunology.
Our business is strong. Total revenue grew to €4.5 billion in 2017. We are more than 7,500 people in all four corners of the globe, inspired by patients and driven by science.
Looking ahead, we have a solid platform for continuous growth with our core products Cimzia®, Vimpat®, Neupro®, Keppra® and Briviact®, and we are preparing the launch of a potential medicine to help patients with osteoporosis. At the same time, we are very excited about the progress in our early research pipeline.