Senior Consultant Real-World Evidence (EU/UK locations)

We are looking to fill the role in Sweden but other EU locations will be considered based on candidates’ skills and experience.

Role context:

A Real-World Evidence Senior Consultant will design and execute real-world evidence (RWE) research studies to provide valuable insights and evidence for pre-clinical portfolio decisions, clinical programs, product reimbursement & access strategies, regulatory and HTA evidence submissions packages. As a RWE Senior Consultant, you will have the opportunity to manage RWE studies to help clients solve strategic, tactical and operational challenges. You will serve on multiple project teams and ensure the delivery on high impact projects to clients. You will have the opportunity to contribute to thought leadership and innovation within projects and practice areas. Finally, and most importantly, you will contribute to put patients first by bringing in real world patient insights throughout the product lifecycle.

Key accountabilities: Provide consultation on data source identification and methodological aspects of observational database analytics Incorporate appropriately latest methodologies and analytic techniques Develop study protocols, methodology/statistical analysis plans, study reports, study publications Lead project task execution by ensuring study progress, organizing project data, communicating appropriately, and coordinating internal and client meetings Manage projects to ensure each is executed according to agreed scope, high quality, and on time Analyze, synthesize, and interpret data findings from studies Communicate effectively research findings to internal and external audiences as needed Provide RWE associates guidance on the implementation of the RWE research studies Project management Client management QualificationsIdeal candidate will possess: Advanced degree (PhD/Masters) in the Data analytics, Programming, Health Informatics, Biostatistics, Epidemiology, Data Science, Decision sciences, Outcomes research A minimum of 5 years’ experience (consulting/pharma) working with in Real-World Evidence, with particular emphasis on large relational databases, processing large administrative healthcare datasets (medical and pharmacy claims), and or clinical databases (Electronic Health Records), creating final analytical databases, conducting secondary data analyses, and developing research study designs Recent Pharmaceutical/CRO experience strongly preferred Extensive experience of project management of RWE, epidemiology, or register studies Experience of business development activities is an advantage Ability to synthesize and communicate findings in a clear and easy to understand form which resonates with audience(s) while maintaining the integrity of key findings Excellent communication skills, both oral and in writing, especially in the relaying of technical information Self-motivation, enthusiasm, ambition and flexibility Fluent English, another European language will be an asset Demonstrated evidence of publications will be viewed favorably