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Principal Neuroscience Researcher, Sensory Explore Innovation
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…observation, formulation of testable hypotheses, experimental design, statistical methods, data analysis and interpretation of…
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HR Business Partner
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Use employee relations data and analytics to identify trends, recommend improvements, and support informed business decisions.
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HR Business Partner
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Drafter, Counter Intrusion
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…OS, an AI-powered operating system that turns thousands of data streams into a realtime, 3D command and control center. As the world enters an era of strategic competition, Anduril is…
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Software Engineer (Full Stack Developer) - Remote
UnitedHealth Group
Austin, TX
- $72,800 to $130,000 USD / year
We are seeking a highly motivated Software Engineer (Full Stack Developer) to design, develop, and support modern enterprise web applications. In this role, you will work across the full…
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Senior Software Engineer - Golang
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Practical experience in data modeling, design and messaging.
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Manager, Data and Analytics Engineering, PricewaterhouseCoopers Advisory Services LLC, Seattle, WA
PricewaterhouseCoopers Advisory Services LLC
Seattle, WA
Design and build scalable data infrastructure and systems to support reliable and efficient data processing, integration, and analysis. Develop and implement end-to-end data pipelines,…
Added 2 mins ago
Senior Director, Global Clinical Development Psychiatry and Neurology
Otsuka Pharmaceutical Development and Commercialization, Inc.
Remote, United States
…MD or Princeton, NJ offices, who will be responsible for the design and oversight of clinical research programs and protocols for OPDC products under good clinical practices…
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Mechanical Designer/Engineer
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AVP, Financial Modeling
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Master's degree in Mathematics, Economics, Data Science, Operations Research, Statistics or related field plus 2 years of experience in a related occupation.
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GIS Cartographer
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Senior COMSEC & Network Engineer (Cloud/Classified)
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Clinical Engineering Data Analyst
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- $32.92 to $45.12 USD / hour
Contributes to development of study design, methods, and data collection approaches as well as grant applications.
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Senior Cost Manager / Quantity Surveyor - Construction Management
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Review and participate with the design services team and general contractor in the development of cost estimates.
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Project Manager - Land Development
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Performs various engineering and design assignments requiring the application of basic principles and fundamental theories studied in a four-year university engineering program, and…
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Software Development Engineer Intern
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Supervisor, Accounts Payable, NA
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The North Face: Senior Coordinator, eCommerce QA/BAV
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Seqirus USA Inc

Manager, CORE

Seqirus USA, MA, United States
Seqirus USA, NJ, United States

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Job details

Posting language: English
Posted: Nov 3, 2026

Original job description

Responsibilities:

Manage and provide technical expertise for Phase IV real-world evidence research across the influenza vaccine portfolio, including the development, coordination, and execution of studies focused on influenza epidemiology, vaccine effectiveness, vaccine safety, burden of disease, vaccine use, and vaccine impact.
Serve as project manager and technical project analyst for assigned internal- and external-facing studies; make scientific, methodological, and operational recommendations; contribute to evidence-generation strategy, regulatory and medical responses, and internal decision-making; and escalate matters with broader portfolio, strategic, or material resource implications.
Develop and review study concepts, protocols, statistical analysis plans, study reports, and internal evidence summaries.
Manage vendors, contract research organizations (CROs), database partners, academic collaborators, and investigators; prioritize competing deliverables; develop contingency plans; and address scientific, operational, methodological, timeline, data, and resource risks to ensure scientifically rigorous, high-quality work within timeline and budget expectations.
Conduct systematic literature reviews, targeted literature searches, qualitative evidence summaries, and meta-analyses to identify evidence gaps and support evidence-generation plans.
Review, interpret, and, where appropriate, conduct statistical analyses of real-world and meta-analytic data in accordance with approved research protocols.
Coordinate scientific dissemination through abstracts, congress presentations, manuscripts, and scientific exchange materials, including drafting and journal submission, coordination of author input, responses to reviewers, data interpretation, presentation development, and scientific review.
Maintain knowledge of relevant literature, real-world evidence trends, epidemiologic methods, reporting standards, leading authorities, academic institutions, government entities, and emerging methodological approaches, and identify opportunities to improve research processes, methods, and evidence-generation approaches.
Participate in CORE, Medical Affairs, and cross-functional project teams and collaborate effectively with internal stakeholders, external experts, professional associations, vendors, and research partners.
Ensure that studies and other company activities comply with applicable epidemiologic reporting and quality standards, including STROBE guidance, ClinicalTrials.gov registration requirements, Institutional Review Board requirements, applicable regulations, and company policies and procedures.

Qualifications:

Graduate degree (Master’s or PhD) in public health, epidemiology, biostatistics, pharmacoepidemiology, health outcomes research, or a related scientific discipline; equivalent relevant experience may be considered.
Minimum of three years of experience in observational research, real-world evidence generation, epidemiology, health outcomes research, or statistical programming using clinical, claims, registry, or electronic health record data.
Strong understanding of Phase IV outcomes research, observational study design, real-world evidence generation, and epidemiologic methods, including comparative effectiveness research, causal inference, confounding control, and vaccine effectiveness methods.
Experience using claims databases, electronic health records, registries, published literature, and other real-world data sources, and conducting systematic literature reviews and meta-analyses.
Experience programming and reviewing statistical analyses using SAS, SQL, R, Stata, or similar software; R programming experience is preferred.
Excellent oral and written communication skills, with the ability to translate complex scientific, epidemiologic, and statistical concepts into clear reports, presentations, publications, and internal evidence summaries.
Demonstrated project-management expertise, including the ability to independently manage multiple priorities, ambiguity, timelines, budgets, and quality expectations while exercising sound judgment.
Ability to establish productive working relationships, collaborate effectively, and build consensus with colleagues, managers, cross-functional teams, vendors, collaborators, and external experts in a global, highly matrixed environment.
Proficiency in Microsoft Word, Excel, and PowerPoint.
Experience in the biopharmaceutical industry, a contract research organization, an academic research setting, or a public health environment is preferred.
Experience in comparative effectiveness research, preferably in vaccinology, infectious diseases, influenza, or respiratory disease, is preferred.
A publication record in peer-reviewed clinical, epidemiologic, health outcomes, or methodological journals is preferred.
Ability to undertake up to 10% domestic and international travel.

About CSL Seqirus CSL Seqirus is part of CSL. As one of the largest influenza vaccine providers in the world, CSL Seqirus is a major contributor to the prevention of influenza globally and a transcontinental partner in pandemic preparedness. With state-of-the-art production facilities in the U.S., the U.K. and Australia, CSL Seqirus utilizes egg, cell and adjuvant technologies to offer a broad portfolio of differentiated influenza vaccines in more than 20 countries around the world. To learn more about CSL, CSL Behring, CSL Seqirus and CSL Vifor visit https://www.csl.com/ and CSL Plasma at https://www.cslplasma.com/.

Our Benefits For more information on CSL benefits visit How CSL Supports Your Well-being | CSL.

You Belong at CSL At CSL, Inclusion and Belonging is at the core of our mission and who we are. It fuels our innovation day in and day out. By celebrating our differences and creating a culture of curiosity and empathy, we are able to better understand and connect with our patients and donors, foster strong relationships with our stakeholders, and sustain a diverse workforce that will move our company and industry into the future. To learn more about inclusion and belonging visit https://www.csl.com/careers/inclusion-and-belonging

Equal Opportunity Employer CSL is an Equal Opportunity Employer. If you are an individual with a disability and need a reasonable accommodation for any part of the application process, please visit https://www.csl.com/accessibility-statement.

Watch our ‘On the Front Line’ video to learn more about CSL Seqirus

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More about this job

Skills

Provide technical expertise
Research
Decision making
Statistics
Presentation skills
Reporting
Electronic health records
SAS
SQL
R
Stata
Communication skills
Project management
Microsoft Word
Microsoft Excel
Microsoft PowerPoint
Communicable diseases

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