Senior Director Immunology Job at SAB Biotherapeutics (Sioux Falls)

Senior Director, Field Medical Affairs Team Lead

We are seeking a highly motivated and experienced Senior Director, Field Medical...

Location

United States

Salary:

Not provided

Cabaletta Bio Inc

Expiration Date

Until further notice

Requirements

Advanced scientific degree (PharmD, PhD, MD, DO) with at least 10 years of experience in the pharma/biotech industry
Minimum of 8 years' experience as a Medical Science Liaison and 3-5 years leading a team of Medical Science Liaisons within the cell therapy space is required
Experience in cell therapy site certifications for commercialization is highly desirable
Therapeutic area expertise in immunology or autoimmune diseases is desirable but not required
Demonstrated ability to build and maintain relationships with internal and external stakeholders, fostering collaboration and alignment
Proven track record of developing and executing medical affairs strategies to support product development, launch, and lifecycle management
Experience with developing and implementing KPIs for field engagement
Expertise in the use of Customer Relationship Management tools (i.e. Veeva CRM)
Excellent communication skills, with the ability to distill complex scientific concepts into clear, concise messages for KOLs and diverse audiences
Familiarity with regulatory requirements and ethical standards governing scientific research and development

Job Responsibility

Leadership & Team Development
Medical Strategy & Execution
KOL & External Engagement
Cross-Functional Collaboration
Pre-Launch & Launch Readiness
Operational Excellence

What we offer

health and retirement
PTO
stock option plans

Fulltime

Senior Director, Molecular Pathology and Cell Biology

Moderna is seeking a strategic and scientifically rigorous leader to serve as Sr...

Location

United States , Cambridge

Salary:

196700.00 - 353400.00 USD / Year

Moderna

Expiration Date

Until further notice

Requirements

PhD, MD, or equivalent in Pathology, Cell Biology, Immunology, Cancer Biology, or related discipline
12+ years of experience in translational research, molecular pathology, or functional cell biology within biotech, pharma, or academia
Strong understanding of advanced tissue-based assay strategies, including highly multiplexed spatial profiling approaches and AI-powered image analysis
Significant experience in cell-based functional assays, including cytotoxicity and immune effector assays
Experience building and deploying advanced experimental model systems (3D cultures, explants, co-culture platforms)
Demonstrated experience supporting translational research programs and contributing to development-stage decision-making
Proven leadership of multidisciplinary scientific teams within a matrixed organization
Strong communication skills and ability to influence across Research and Development functions

Job Responsibility

Lead and integrate high-performing Molecular Pathology and Cell Biology teams while defining and executing a forward-looking translational strategy aligned with therapeutic area priorities and portfolio needs
Serve as a scientific thought partner to Research, Translational Medicine, and Clinical Biomarker leaders, shaping priorities and enabling effective cross-functional collaboration
Set the strategic direction for Molecular Pathology support of target and tissue expression profiling across normal and disease tissues to inform target selection, program prioritization, and translational hypothesis development
Guide the deployment of routine and advanced tissue-based assays, novel spatial profiling approaches, and the continued evolution of the digital pathology infrastructure to ensure fit-for-purpose application across programs
Oversee development and execution of cell-based functional assays including cytotoxicity, cell-killing, ADCC, and pathway interrogation assays
Drive innovation in advanced experimental model systems including organoids, patient-derived explants, and co-culture systems
Establish quality standards, reproducible workflows, and scalable infrastructure to deliver high-quality data supporting Therapeutics Research, Translational Medicine, and, when appropriate, IND-enabling efforts

What we offer

Best-in-class healthcare coverage, plus voluntary benefit programs
A holistic approach to well-being, with access to fitness, mindfulness, and mental health support
Family planning benefits, including fertility, adoption, and surrogacy support
Generous paid time off, including vacation, volunteer days, sabbatical, global recharge days, and a discretionary year-end shutdown
Savings and investment opportunities to help you plan for the future
Location-specific perks and extras
Eligible for an annual discretionary bonus, other incentive compensation, or equity award

Fulltime

Senior Director – BioIntelligence

The AI & Data for Engineered Biologics (AIDE) organization at Amgen is seeking a...

Location

United States , Thousand Oaks

Salary:

239775.00 - 295217.00 USD / Year

Amgen

Expiration Date

Until further notice

Requirements

Doctorate degree in Computational Biology, Machine Learning, Bioinformatics, Computer Science, Biophysics, or related field and 5 years of experience applying machine learning or computational modeling to biological systems
OR Master’s degree in Computational Biology, Machine Learning, Bioinformatics, Computer Science, Biophysics, or related field and 9 years of experience applying machine learning or computational modeling to biological systems
OR Bachelor’s degree in Computational Biology, Machine Learning, Bioinformatics, Computer Science, Biophysics, or related field and 11 years of experience applying machine learning or computational modeling to biological systems
At least 5 years experience directly managing people and/or leadership experience leading teams, projects, programs, or directing the allocation or resources

Job Responsibility

Lead the BioIntelligence Team within our Large Molecule Discovery organization, defining strategy and priorities for AI-driven biologics modeling
Develop and execute a roadmap for machine learning and AI approaches that accelerate engineered biologics discovery
Align BioIntelligence capabilities with broader Research and Large Molecule Discovery priorities
Oversee development of predictive models for key biologics properties, including developability, stability, manufacturability, and immunogenicity
Advance modeling approaches using modern AI techniques such as: protein language models
generative modeling and inverse folding
representation learning
active learning and Bayesian optimization
Guide the use of multimodal biological datasets including sequence, structure, and experimental assay data
Lead development of production-quality research software and deployable ML models used across discovery teams

What we offer

A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts
A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan
Stock-based long-term incentives
Award-winning time-off plans
Flexible work models where possible

Fulltime

Senior Director, Seasonal Vaccines

You will help set scientific strategy for a seasonal viral vaccine program based...

Location

United States , Pearl River

Salary:

214900.00 - 341100.00 USD / Year

Pfizer

Expiration Date

Until further notice

Requirements

PhD in Virology or a related field
10+ years industry or biotech experience in pre-clinical research and in vaccine technical development, with basic scientific expertise in SARS-CoV-2 research, immunology, serology, RNA vaccine technologies, and synthetic virology
Practical knowledge of global SAR-CoV-2 surveillance, recommendation, and regulatory systems
Experience providing scientific leadership for projects in the pharmaceutical industry, and proven track record of project advancement and delivery in vaccines
Global scientific reputation as evidenced by publication record and interaction with NIH or other established government research agencies
Understanding the scientific and non-scientific aspects of vaccines, and viral vaccine scientific, clinical and competitive landscape
Demonstrated innovation and experience to applying knowledge, techniques and skills to identify and validate best new technologies
Strong communication skills including public speaking experience and scientific writing
Experience collaborating cross functionally
Scientific analysis experience

Job Responsibility

Support and enhance the current infrastructure and processes required to enable robust and rapid development and licensure of variant-adapted COVID-19 vaccines
Represent Research on the cross-functional Vaccine Product Team, operating at the interface between research and development and coordinating with non-research functions to meet program goals, including life cycle management
Establish relationships with and serve as a primary scientific liaison with external alliance partners, including collaborating companies, government agencies and non-governmental organizations
Actively manage project risks, devising and implementing appropriate mitigation activities with multidisciplinary teams
Lead timely and effective communication of project risks and impact to senior leaders
Ensures that intellectual property is appropriately obtained and safeguarded
Take a key role in communication about vaccine programs in internal Pfizer documents and external patent applications, regulatory submissions, scientific papers, and conferences
Leads a motivated, committed and engaged research team to provide preclinical data to support annual strain change activities as well as exploration of next-generation vaccine technologies, leading direct reports and non-reports, reviewing experimental designs and data

What we offer

eligibility for participation in Pfizer’s Global Performance Plan with a bonus target of 22.5% of the base salary
eligibility to participate in our share based long term incentive program
401(k) plan with Pfizer Matching Contributions and an additional Pfizer Retirement Savings Contribution
paid vacation, holiday and personal days
paid caregiver/parental and medical leave
health benefits to include medical, prescription drug, dental and vision coverage
Relocation Support Available

Fulltime

National Value and Market Access Manager

The National Value & Market Access Manager is a strategic role responsible for d...

Location

United Kingdom , Mechelen

Salary:

Not provided

Alfasigma

Expiration Date

Until further notice

Requirements

Degree in Life Sciences, Pharmacy, Health Economics, or related field (advanced degree preferred)
Significant experience in Market Access, tendering or Pricing within the UK pharmaceutical/biotech sector
HCP and Payer facing experience in the UK or Ireland pharmaceutical sector (preferred)
Proven track record of leading HTA submissions with deep knowledge of NICE, SMC, NCPE and HSE appraisal processes and cost-effectiveness frameworks
Strong expertise in pricing, reimbursement, and tender processes
Experience in developing and implementing national and regional access strategies
Proven experience & success in regional market access & NHS engagement, ideally within immunology and hepatology

Job Responsibility

Lead access planning across Alfasigma product portfolio lifecycle stages, including pre-launch, early access (if appropriate), launch, and post-launch optimisation
Lead all HTA dossier submissions (e.g., NICE, SMC, NCPE) and national/regional tenders across UK & Ireland, ensuring quality, timely delivery, and alignment with strategic objectives
Collaborate cross-functionally (Medical, HEOR, Regulatory, Commercial) to generate robust value propositions and evidence packages
Lead UK & Ireland pricing strategy across the commercial portfolio in collaboration with the GM and Global Team, ensuring robust governance, regulatory compliance, and alignment with company policies
Identify and mitigate access risks related to reimbursement, budget impact, policy changes, or competitive dynamics
Collaborate with commercial and supply teams to optimise tender outcomes and contract performance
In collaboration with the Senior Commercial Director, develop and lead national and regional market access strategies
In line with the national and regional access strategies, develop associated value messaging, tools and resources for implementation by the Regional Access Team
Support the Regional Access Managers with the insights, training, and resources required to execute access strategies effectively
In collaboration with the brand team, support Value Proposition & Evidence Generation by defining and articulating product value propositions tailored to UK payers and NHS stakeholders

What we offer

competitive salary
comprehensive benefits
extensive opportunities for professional growth and development

Fulltime

Statistics Director, Oncology

At GSK, we have bold ambitions for patients, aiming to positively impact the hea...

Location

United Kingdom; United States , London; Stevenage; Collegeville

Salary:

Not provided

GSK

Expiration Date

Until further notice

Requirements

Master's degree in Statistics, Biostatistics or related field with relevant industry experience and a proven track record of innovation and strategic influence
Prior experience in Oncology
Experience with advanced methodologies such as Bayesian approaches, longitudinal modelling, causal inference or machine learning
Demonstrated leadership in a matrix environment, influencing senior stakeholders and cross-functional teams
Experience leading statistical activities from protocol design through final analysis and dissemination
Proven experience with regulatory interactions and preparation of statistical sections for submissions
Strong written and verbal communication skills, able to explain statistical concepts to diverse audiences

Job Responsibility

Lead statistical strategy for one or more key Oncology programs across phases of clinical development and lifecycle activities, ensuring alignment with business objectives and scientific rigor
Act as the statistical lead in cross-functional project teams and in interactions with regulatory authorities
Design robust clinical trials and observational analyses and approve analysis plans and final statistical reporting
Provide technical leadership, mentoring and development for statisticians and statistical programmers
Drive improvements in statistical methods, standards, and governance for immunology projects
Champion innovation by introducing cutting-edge approaches that enhance project outcomes
Collaborate with other statistical leaders within the company to drive a culture of innovation and continuous learning

What we offer

Competitive base salary
Annual bonus based on company performance
Flexible working options available for most roles
Learning and career development
Access to healthcare & wellbeing programmes
Employee recognition programmes

Fulltime

Target Validation Sr Director

This research based Senior Director role will be responsible for building, leadi...

Location

United States , South San Francisco

Salary:

265405.00 - 312459.00 USD / Year

Amgen

Expiration Date

Until further notice

Requirements

Doctorate degree PhD in biochemistry, cell biology, molecular biology, computational biology, immunology, oncology, metabolism or a relevant discipline and 7 years of scientific leadership experience in biotech, pharma or equivalent research environments
OR Master’s degree in biochemistry, cell biology, molecular biology, computational biology, immunology, oncology, metabolism or a relevant discipline and 10 years of scientific leadership experience in biotech, pharma or equivalent research environments
OR Bachelor’s degree in biochemistry, cell biology, molecular biology, computational biology, immunology, oncology, metabolism or a relevant disciplineand 12 years of scientific leadership experience in biotech, pharma or equivalent research environments

Job Responsibility

Lead and develop a multidisciplinary organization of ~25 scientists within Research Biology
Integrate diverse experimental disciplines and workflows to ensure coordinated execution and efficient delivery of novel molecular insights
Establish platform priorities, resource allocation, and capacity planning in alignment with Research Biology and Therapeutic Area priorities
Define clear roles, responsibilities, and seamless handoffs across teams and partnering organizations
Drive adoption of automated experimental workflows, and integration of AI/ML to enable efficient experimentation across programs
Serve as a senior scientific partner to Target Discovery and Therapeutic Areas
Set clear expectations and enable scientists with diverse skill sets to collaborate effectively and contribute to early research pipeline
Serve as a core member of Target Discovery Advisory Forum, and play a key role in target discovery, validation and prioritization. Engage, influence, and align therapeutic area stakeholders
Guide team members in synthesizing and communicating complex scientific and data-driven insights to key stakeholders and advisory forum
Contribute to fostering a highly collaborative, creative, dynamic and cutting-edge research environment

What we offer

competitive benefits
collaborative culture
health and welfare plans for staff and eligible dependents
financial plans with opportunities to save towards retirement or other goals
work/life balance
career development opportunities
Retirement and Savings Plan with generous company contributions
group medical, dental and vision coverage
life and disability insurance
flexible spending accounts

Fulltime

Director, Insights and Analytics

The Director, Insights & Analytics will lead the development of Cabaletta’s comm...

Location

United States , Philadelphia

Salary:

Not provided

Cabaletta Bio Inc

Expiration Date

Until further notice

Requirements

Bachelor’s degree in life sciences, business, marketing, or a related field
advanced degree (MBA, PharmD, MS) preferred
8 years of experience in pharmaceutical/biotech insights, analytics, or commercial strategy
Experience in rare disease, immunology, autoimmune disease, or cell therapy strongly preferred
Demonstrated expertise in: Primary market research
Competitive intelligence
Forecasting and market modeling
Strategic analytics
Strong ability to translate complex scientific and market data into strategic insights
Exceptional communication and executive presentation skills

Job Responsibility

Build and operationalize Cabaletta’s insights & analytics function from the ground up, including defining the operating model, selecting tools and vendors, and establishing repeatable processes for insight generation and decision support
Develop and lead Cabaletta’s commercial insights and analytics strategy across priority autoimmune indications
Translate market data, physician insights, and treatment dynamics into actionable recommendations for leadership
Provide decision support to the Chief Business Officer and executive leadership team on portfolio strategy, indication prioritization, and commercialization planning
Design and execute primary market research with key stakeholders including physicians, payers, patients, and advocacy groups
Generate insights on diagnostic pathways, treatment algorithms, unmet needs, and adoption drivers across autoimmune diseases
Partner with clinical and medical teams to ensure commercial insights inform trial design, endpoints, and value propositions
Establish and lead a competitive intelligence capability across autoimmune cell therapy, biologics, and emerging modalities
Monitor scientific, clinical, regulatory, and commercial developments in competing programs
Deliver executive-level competitive insights to inform strategic positioning and launch planning

What we offer

health and retirement
PTO
stock option plans

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Senior Director Immunology

Job Description

Job Responsibility

Requirements

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