Associate Director Epidemiology
Associate Director Epidemiology
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Salary Not Disclosed
1 Vacancy
Job Description
When we put unexpected teams in the same room we unleash bold thinking with the power to inspire lifechanging medicines. Inperson working gives us the platform to connect work at pace and challenge perceptions. Thats why we work on average a minimum of three days per week from the office. But that doesnt mean were not flexible. We balance the expectation of being in the office while respecting individual flexibility. Join us in our unique and ambitious world.
Introduction to role
The Associate Director Epidemiology is a strategic and scientific leader responsible for developing coordinating and completing impactful epidemiology deliverables within the Koselugo program. This role involves overseeing the development incorporation and analysis of Alexions studies either personally or through the management of other Epidemiologists or vendors/contractors. The goal is to enhance the understanding of disease natural history treatment outcomes and drug safety evaluations. The Associate Director will ensure all deliverables are completed efficiently within budget and with high quality and accuracy.
The Associate Director will participate in crossfunctional teams and lead subteam meetings as needed. This role involves closely working with collaborators from Clinical Development Patient Safety Regulatory Affairs Medical Affairs and Commercial. The ideal candidate will have experience in analyzing and interpreting epidemiologic data within the context of rare diseases and a passion for applying epidemiology to support lifetransforming therapies for patients.
Accountabilities
- Responsible for developing and completing Epidemiology deliverables associated with the Koselugo program
- Coordinate and oversee the planning and of analyses from Koselugo studies. Provide oversight and guidance to statisticians and programmers in developing analytic deliverables.
- Propose design initiate complete and report epidemiologic study analyses conducted within observational studies registries or external databases for assigned indications
- Summarize results in written reports and oral presentations
- Provide epidemiology support to Clinical Development Patient Safety Regulatory Affairs Medical Affairs and Commercial activities across the development life cycle. Actively participate in crossfunctional therapeutic area teams and lead subteam meetings as appropriate
- Provide epidemiology perspective into study protocols case report forms (CRFs) and regulatory documents for assigned indications
- Interact with authors and inhouse reviewers on scientific manuscripts clinical conference abstracts presentations and posters based on data from observational studies
- Represent Epidemiology and Real World Science department during interactions with key external customers like Scientific Advisory Boards and regulatory authorities
- Critically appraise and synthesize relevant epidemiological literature
- Maintain awareness of epidemiology with respect to regulatory requirements payer trends and advancement of pharmacoepidemiology methods
- Travel may be required (up to 10
Essential Skills/Experience
- At least 3 years of industry experience in the pharmaceutical industry biotechnology or consulting environment for Doctorallevel candidates or 6 years of industry experience for Masterslevel candidates
- PhD / DSc / DrPH in Epidemiology with 3 years of industry experience OR MPH / MSc in Epidemiology with 6 years of industry experience
Desirable Skills/Experience
- Excellent oral and written communication skills
- Knowledge of drug and clinical development process
- Excellent attention to detail and quality and scientific rigor
- Ability to work under pressure and lead by example
- Strong interpersonal skills and ability to work effectively in multidisciplinary teams
- Thorough and uptodate technical knowledge of epidemiology and biostatistics methods
- Experience and familiarity using SAS for statistical analysis
- Record of highquality publications in peerreviewed journals
At Alexion you will find a collaborative culture that encourages innovation and a diverse environment where your contributions are valued. You will have the opportunity to be at the forefront of rare disease research and make a meaningful difference in patients lives.
Ready to lead and inspire Apply now and take the first step towards a fulfilling career at Alexion AstraZeneca Rare Disease.
#LIHybrid
Date Posted
03Apr2025Closing Date
16Apr2025Alexion is proud to be an Equal Employment Opportunity and Affirmative Action employer. We are committed to fostering a culture of belonging where every single person can belong because of their uniqueness. The Company will not make decisions about employment training compensation promotion and other terms and conditions of employment based on race color religion creed or lackthereof sex sexualorientation age ancestry national origin ethnicity citizenship status marital statuspregnancy (including childbirth breastfeeding or related medical conditions) parental status (including adoption or surrogacy) military status protected veteran status disability medical condition gender identity or expression genetic information mental illness or other characteristics protected by law. Alexion provides reasonable accommodations to meet the needs of candidates and employees. To begin aninteractive dialogue with Alexion regarding an accommodation please contact . Alexion participates in EVerify.
Required Experience:
Director
Employment Type
Full-Time
