Senior Consultant bei Alirahealth

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Join our global team dedicated to innovation and initiative, where physical walls and different time zones don’t limit, but encourage, collaboration. Where all contributions and new ideas are explored with an open mind and work is driven by our shared values: be courageous, be accountable, be honest, be inclusive and elevate others.

Job Description Summary

Job Description

(Senior) Consultant in Real-World Solutions team at Alira Health

 

(SENIOR) CONSULTANT IN THE REAL-WORLD EVIDENCE TEAM

JOB DESCRIPTION

 

Job Title:        (Senior – TBD) Consultant                                       

Reports to:    Associate Director, Real-World Evidence

Location:       Flexible (EU)

                       

ABOUT ALIRA HEALTH

At Alira Health, our mission is to enable healthcare transformation. We support our clients with a technology-enabled integrated suite of Product Development, Regulatory, Clinical, Global Market Access, Real-World Evidence, Patient Engagement, Strategy Consulting, and Transaction Advisory services. Our team of scientists, strategists, bankers, and physicians collaborate to fully understand every aspect of our clients’ businesses and offer a continuum of support to uncover opportunities, accelerate innovation, and improve outcomes for patients around the world.

Our clients are global, and so are we. Our local presence and global collaboration allow us to deliver actionable business insights and an unmatched continuity of support across the full corporate and product lifecycle. We mostly operate across ten offices located in Boston, and Cambridge, MA and San Francisco, CA in the US, Toronto in Canada, and Barcelona, Basel, London, Milan, Munich, and Paris in Europe.

 

REAL-WORLD EVIDENCE

At Alira Health, our Real-World Evidence (RWE) team is deeply integrated with key practices across the organization, including Patient-Centered Technology Solutions, Market Access, Patient Engagement, Medical Strategy, Regulatory, Clinical, and Biometrics. Our RWE practice encompasses the full spectrum of real-world evidence needs—from study design and execution to effective communication—catering to all customer segments.

With a strong presence in Barcelona, Basel, Paris, and Boston, our team of multidisciplinary experts brings extensive knowledge across data scient, statistics, analytics, epidemiology, health economics, outcomes research, and Real-World Data (RWD). This diverse expertise allows us to deliver impactful insights and innovative solutions to our pharmaceutical clients.

 

REAL-WORLD SOLUTIONS ACTIVITY

The RWE team supports a variety of clients in the life sciences industry, mainly manufacturers, and works closely with clients in Europe and the USA. One of our main activities is to support the design and execution of real-world observational studies. These include secondary data sources or, from the primary collection of RWD, leveraging either the Alira Health’s digital health solutions that allow us to collect data directly from patients, or the Alira Health Clinical Operations team. Secondly, we also support our clients in designing strategic integrated evidence plans that include RWE, supporting the value demonstration of technologies.

 

THE CONSULTANT ROLE                                                             

As a consultant, you will work on client projects as part of a team, interacting closely with an Associate Director of the Real-World Solution team. You will combine your skills in epidemiology, and public health (or related) together with your strong interest and/or expertise in the Healthcare / Life Sciences industry, to take part in projects and ensure that the available real-world data are leveraged appropriately.

You will play a key role in developing study protocols, interpreting data study reports, and communication materials e.g., abstracts, posters, and manuscripts.

Responsibilities include but are not limited to supporting the development of RWE proposals and presentations, RWE study design, statistical analyses, literature searches, communications, and medical writing.

 

DESIRED SKILLS AND EXPERIENCE

·       Bachelor’s or Master’s in Epidemiology, Data Science, or related field

 

·       Experience managing client and internal RWE projects (pharma or consulting) with strong project management and communication skills

 

·       Knowledge of regulatory guidelines (FDA, EMA, HTA) for RWE and epidemiology

 

·       Proven experience in epidemiological research, study design, and data analysis; plus for CER, post-marketing commitments, and external control arm studies

 

·       Skilled in leveraging diverse RWD sources to execute RWE studies (protocols, reports, manuscripts); prior knowledge of SNDS, PMSI, UK Biobank, CPRD and other claims databases a strong plus

 

·       Basic statistical knowledge with ability to contribute to analysis plans

 

·       Proficiency in R, SAS, or Python for statistical analysis

 

·       Ability to interpret and communicate findings to stakeholders, including regulatory bodies, providers, and patients

 

·       Strong analytical, organizational, and interpersonal skills with attention to detail

 

·       Excellent written and verbal communication in English

 

·       Proficiency in Microsoft Office (Excel and PowerPoint essential)

 

Languages

English

Education

Bachelor of Science (BS): Business Administration/Management, Bachelor of Science (BS): Economics, Bachelor of Science (BS): Finance, Bachelor of Science (BS): Life Sciences

Contract Type

Regular Jetzt bewerben