Real World Evidence Epidemiologist
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Søborg
Epidemiologist with expertise in Real World Evidence in Clinical Trials Are you looking for an opportunity to work in a highly professional, scientific, and global environment where you can use your solid epidemiological skills working with Real World Data in Clinical Trials? And are you ready to join a team of data scientists and epidemiologists using advanced epidemiological methods to improve people’s lives? Then this may be your opportunity to pursue an exciting career in a global organisation! A pply today for a life-changing career. The position This is a new position focusing on the methodology of using Real-World Data in relation to Clinical Trials. Together with stakeholders from across the organisation, you will drive the implementation of novel ways of generating and combining evidence across our portfolio. Your main responsibilities will be: Advising your stakeholders on subjects like augmentation, target trial emulations, innovative trial design, tokenisation, and data linkage and setting new standards for doing so. To apply expert knowledge and experience of integrating Real-World Evidence with Clinical Trial data and how to leverage Real-World Evidence in a Clinical Trial. To identify and determine efficient data collection approaches and data sources relevant for the questions being investigated. To perform and guide complex epidemiological activities and participate in working groups requiring pharmacoepidemiology expertise. Moreover, you will be part of setting direction for epidemiology activities in . You will be interacting with many stakeholders – either when communicating epidemiological considerations and results to internal stakeholders or through contact with research organisations, commercial partners and academic institutions involved in analysis of epidemiological data. Qualifications To be successful in this role, we are looking for candidates with the following qualifications: MD, DVM, or hold a master’s degree in public health, life sciences, biostatistics, or equivalent. Strong Epidemiological background Solid hands-on experience in combining Real-World Evidence and Clinical Trial data. Experience with data linkage, trial augmentation, innovative trial designs and tokenisation. Experience within pharmacoepidemiology from the pharmaceutical industry or consulting. Experience from working with regulatory authorities. Additional preferred qualifications: A PhD degree in a related field. We expect you to be ambitious and innovative. It is essential that you can use your good interpersonal and communication skills to achieve results together with others, both internally and when working with external project teams. You must thrive in a role where you have responsibility, you are proactive and work independently. The job is globally oriented and excellent communication skills together with interest in co-operating with stakeholders across the globe is a must. About the department In Development, we are responsible for managing clinical drug development worldwide from early development phases to product launch and beyond. We provide medical and scientific documentation for clinical submissions and authorities while ensuring that the process lives up to global standards, regulations, and business ethics. The department of Real-World Science is part of Data Science in Development and located in Søborg, Denmark. The department focus on insights and causal relationships from real world data (RWD) through advanced statistical methods. We analyse many different data sources to generate evidence to support clinical drug development projects and launched products. You will be joining a team of highly professional, engaged, and motivated data scientists and epidemiologists. Working at At , we don’t wait for change. We drive it. We’re a dynamic company in an even more dynamic industry, and we know that what got us to where we are today is not necessarily what will make us successful in the future. We embrace the spirit of experimentation, striving for excellence without fixating on perfection. We never shy away from opportunities to develop, we seize them. From research and development, through to manufacturing, marketing, and sales – we’re all working to move the needle on patient care. Contact For further information, please contact Camilla Birkegård at (hiring manager). Deadline April 1st, 2024 You do not need to attach a cover letter to your application, but please include a few sentences about why you are applying in your resume or CV. To ensure an efficient and fair recruitment process, please refrain from adding a photo in your CV. We commit to an inclusive recruitment process and equality of opportunity for all our job applicants. At we recognize that it is no longer good enough to aspire to be the best company in the world. We need to aspire to be the best company for the world and we know that this is only possible with talented employees with diverse perspectives, backgrounds and cultures. We are therefore committed to creating an inclusive culture that celebrates the diversity of our employees, the patients we serve and communities we operate in. Together, we’re life changing.
Information og data
Denne ledige stilling har jobtypen "Softwareudvikler", og befinder sig i kategorien "Informationsteknologi".
Arbejdsstedet er beliggende i Søborg.
Jobbet er oprettet på vores service den 12.3.2024, men kan have været deaktiveret og genaktiveret igen.
Dagligt opdateret: Dette job opdateres dagligt ud fra jobudbyderens hjemmeside via vores søgemaskineteknologi og er aktivt lige nu.
- Softwareudvikler
- Søborg
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