Senior Statistician Job at UC San Diego (La Jolla)

Senior Medical Statistician

Does supporting world-class research and improving lives of patients excite you?...

Location

Salary:

Not provided

MTM Pet Care (LECVNG)

Expiration Date

Until further notice

Requirements

A first or post-graduate degree in statistics or equivalent subject
A minimum of five years’ work experience in medical statistics
Excellent statistical modelling skills and the ability to interpret analysis results
Sound IT skills and programming experience using statistics software such as STATA, SAS or R
Excellent oral and written communication skills
Experience with epidemiological studies or health care databases
Experience in designing and conducting analysis for randomised controlled trials
Evidence of peer reviewed publications
Some knowledge of health economics

Job Responsibility

Provide statistical input to research proposals and protocols for academic and commercial clients, tasks including: Study design
Sample size and power calculations
Plan and conduct statistical analysis
Statistical methodology
Act as the lead statistician on assigned research projects undertaking tasks including: Develop data cleaning processes and imputation strategy as required
Conduct or supervise exploratory data analysis of datasets and baseline variables
Conduct statistical analyses of study outcomes and assist in the interpretation of results
Contribute to the final statistical analysis report (including production of summary tables and figures)
Contribute to journal publications and conference abstracts and posters
Carry out quality tasks for other research team members

Vice president global head of statistics vcrd

Pfizer is seeking a Vice President, Global Head of Statistics to join our thrivi...

Location

United States , Pearl River; Collegeville

Salary:

274000.00 - 426800.00 USD / Year

Pfizer

Expiration Date

Until further notice

Requirements

Advanced degree in statistics, biostatistics, or related field required. PhD preferred.
15+ years of experience in drug development
5-10 years of experience in vaccine development
At least 5 years of managerial experience in drug development
Capability to provide statistical leadership to cross-functional teams and the ability to both communicate and influence the biostatical perspective to diverse audiences
Effective verbal and written communication skills relating to colleagues and associates both inside and outside the organization
A compelling and inspiring leadership style with a sharp scientific mind, who combines broad knowledge and understanding of biological systems and statistics. A world-class leader in his/her field.
Ability to perform sophisticated mathematical and statistical calculations, and to perform complex data analysis
Disaggregates complex problems to facilitate problem solving
Adept at distinguishing the relevance of information inputs to the decision-making process

Job Responsibility

Sets the vision and leadership for providing the highest level of data management, modeling, and statistical advice across the function to senior Vaccines Research and Development (VRD) leadership
Is accountable to lead the necessary stakeholders to plan, direct and coordinate a large and expanding portfolio of specialized and complex Vaccine Research and Development (VRD) projects spanning phase 1 through phase 4 clinical development
Must have the broadest knowledge of clinical data management and statistical analysis tools and interpret results from clinical, non-clinical, modelling and simulation, and epidemiologic studies
Is accountable to develop and roll out new initiatives and lead the VCRD Statistics group in strategic planning
Leads the activities of Senior Directors directing the statisticians and modelers in VCRD and at Functional Service Providers
Provides senior management review of protocols and CSRs, and is the senior representative to internal review committees, DMC-related company steering committees, etc.
Influences cross functional (TA) activities, in a consultative role, and provides the SVP of Clinical Research with more strategic advice as to the present and future direction for the VCRD Statistics group
Provides the highest level of strategic and statistic leadership to VRD leadership and the full vaccine portfolio
Lead and inspire the VRD statistics organization to provide the highest level of statistical and modeling support. Evaluates the material generated by supervised staff including senior director reports for validity, quality, and effectiveness of presentation and coaches them in preparation for regulatory and Key Opinion Leader interactions.
Provide senior management statistical review of key documents (protocols, CSRs, regulatory briefings)

What we offer

eligibility for participation in Pfizer’s Global Performance Plan with a bonus target of 30.0% 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

Statistician, Research

We’re seeking an experienced Statistician to Leverage varied statistical experie...

Location

United States

Salary:

90000.00 - 125000.00 USD / Year

Loyal

Expiration Date

Until further notice

Requirements

MS in statistics, biostatistics, or a related field
4+ years of industry experience with statistical analyses in a biotech or pharmaceutical setting
Proficient programming skills (R, python) and version control (git)
Experience developing reproducible analysis workflows and documentation (e.g., quarto or Jupyter notebooks)
Strong written and verbal scientific communication skills
Demonstrated interest in aging biology, longevity science, or age-related disease
Familiarity with Google Workspace applications (e.g., Sheets, Slides, etc.)

Job Responsibility

Working closely with senior statisticians, biologists, and clinicians to perform statistical analyses for preclinical and clinical investigations
Supporting experimental design using simulation- and equation-based power and sample size analyses
Applying a variety of statistical analysis techniques to our studies, including GLMs, survival analysis, longitudinal/mixed effects modeling
Contributing to documentation that is sent to regulatory agencies, including study protocols, study reports, statistical analysis plans and data package documentation
Collaborating with data engineers and laboratory and clinical research teams to advise on data collection and database infrastructure
Sharing scientific results for internal meetings/presentations, manuscripts, or poster sessions and conference presentations
Assisting in endpoint and/or assay development through exploratory data analysis and modeling
As the team grows, contributing to the mentorship and training of more junior bioinformaticians and supporting best practices in analysis and reproducibility

What we offer

Full-coverage health insurance — medical, dental and vision — for you and your dependents
$1,000 home office equipment stipend
$1,200/year learning budget for books, courses, etc.
$250/month wellness budget for gym, cleaners, spa, food, etc.
All 3-day weekends are turned into 4-day weekends
Unlimited vacation and paid holidays
Paw-ternity leave — adopt a dog and get a day off with your new family member
Competitive salary
Company equity options grant for new hires

Fulltime

Principal Statistician

The Principal Statistician will provide senior-level statistical expertise to su...

Location

United Kingdom

Salary:

Not provided

GT

Expiration Date

Until further notice

Requirements

Senior-level expertise in clinical trial statistics within biotech or pharmaceutical environments
Strong hands-on statistical programming experience
Deep understanding of advanced statistical methodologies
Experience supporting regulatory submissions and inspection-ready deliverables (FDA / EMA)
Ability to work independently in a fast-paced, evolving organisation

Job Responsibility

Provide senior statistical expertise for the design, analysis, and interpretation of clinical trials across clinical development programs
Define statistical strategies including estimands, sample size, interim analyses, and analytical approaches
Perform hands-on statistical programming and review of analysis datasets, tables, figures, and listings
Apply advanced statistical methodologies and ensure alignment with regulatory expectations
Support the definition, analysis, and interpretation of ophthalmology-specific clinical endpoints
Ensure high-quality, accurate, and inspection-ready statistical deliverables
Collaborate closely with Clinical, Medical, Regulatory, Data Management, and Biometrics teams
Contribute to statistical sections of protocols, SAPs, clinical study reports, and regulatory documents
Act as a statistical thought partner, clearly communicating results and implications to non-statistical stakeholders

What we offer

Health insurance
Psychotherapy coverage
Sport coverage
Learning budget
18 business days of paid vacation days per year
Paid sick leaves
All public holidays are paid days off

Fulltime

Director, Energy Markets and Security

The IEA seeks to recruit a Director to lead the Directorate of Energy Markets an...

Location

France , Paris

Salary:

16090.00 EUR / Month

IEA

Expiration Date

March 10, 2026

Requirements

An advanced university degree in engineering, economics, energy economics or equivalent in a relevant field
At least 15 years’ experience shaping and implementing international energy policy, including experience in government and in international or intergovernmental contexts
Excellent knowledge of the energy sector, oil gas and electricity markets, industries, technologies and government energy policy-making and regulation
Excellent knowledge of oil and gas markets is essential to support the Agency’s oil market and emergency preparedness work
Well-established professional network across relevant stakeholders
Fluency in English, one of the two OECD official languages, and a knowledge of, or willingness to learn, French

Job Responsibility

Lead the Directorate in delivering the programme of work in line with Member priorities, the Executive Director’s guidance and the IEA Programme of Work and Budget
Provide strategic direction for the Agency’s short- and medium-term analysis of global energy markets (oil, gas, electricity and critical minerals), emergency preparedness and energy market regulation, and policies supporting the deployment of renewable energy
Identify and respond to emerging energy security challenges, including disruptions to oil supply, and develop and implement actions and strategies through which the Directorate can assist member and non-member countries to respond to these challenges
Ensure the Directorate is at the forefront of international analysis on energy markets, in line with current developments and emerging trends, and shaping the IEA’s global contribution
Oversee Directorate reports and programme proposals ensuring that they make an effective contribution to the policy process (national and international) and that they are consistent with the Agency’s overall strategy and messages
Represent the Directorate and the Agency (Secretariat) at senior level with member governments of the Agency, bilaterally and multilaterally, as well as with other international institutions in the energy field, with the private sector and with representatives of civil society
Promote global dialogue and co-operation on energy markets, energy security and emergency policy issues and measures with member governments, major consuming and producing countries and international organisations such as OPEC, IEF, IRENA, and the G20
Ensure effective co-operation with energy industry stakeholders including the international oil and gas industry through the IEA’s Industry Advisory Board (IAB), the coal industry through the Coal Industry Advisory Board (CIAB) and the renewable industry through the Renewable Industry Advisory Board (RIAB)
Lead high-level missions to member and partner countries, engaging Ministers and senior policy makers
Lead and develop a Directorate, of over 110 staff (analysts, statisticians, support and consultants) through merit-based recruitment, professional development, and performance management

What we offer

Monthly base salary starting from 16 090 EUR plus allowances, based on eligibility, exempt of French income tax

Fulltime

!

Director, Energy Markets and Security

The IEA seeks to recruit a Director to lead the Directorate of Energy Markets an...

Location

France , Paris

Salary:

16090.00 EUR / Month

IEA

Expiration Date

March 10, 2026

Requirements

An advanced university degree in engineering, economics, energy economics or equivalent in a relevant field
At least 15 years’ experience shaping and implementing international energy policy, including experience in government and in international or intergovernmental contexts
Excellent knowledge of the energy sector, oil gas and electricity markets, industries, technologies and government energy policy-making and regulation
Excellent knowledge of oil and gas markets is essential to support the Agency’s oil market and emergency preparedness work
Well-established professional network across relevant stakeholders
Fluency in English, one of the two OECD official languages, and a knowledge of, or willingness to learn, French

Job Responsibility

Lead the Directorate in delivering the programme of work in line with Member priorities, the Executive Director’s guidance and the IEA Programme of Work and Budget
Provide strategic direction for the Agency’s short- and medium-term analysis of global energy markets (oil, gas, electricity and critical minerals), emergency preparedness and energy market regulation, and policies supporting the deployment of renewable energy
Identify and respond to emerging energy security challenges, including disruptions to oil supply, and develop and implement actions and strategies through which the Directorate can assist member and non-member countries to respond to these challenges
Ensure the Directorate is at the forefront of international analysis on energy markets, in line with current developments and emerging trends, and shaping the IEA’s global contribution
Oversee Directorate reports and programme proposals ensuring that they make an effective contribution to the policy process (national and international) and that they are consistent with the Agency’s overall strategy and messages
Represent the Directorate and the Agency (Secretariat) at senior level with member governments of the Agency, bilaterally and multilaterally, as well as with other international institutions in the energy field, with the private sector and with representatives of civil society
Promote global dialogue and co-operation on energy markets, energy security and emergency policy issues and measures with member governments, major consuming and producing countries and international organisations such as OPEC, IEF, IRENA, and the G20
Ensure effective co-operation with energy industry stakeholders including the international oil and gas industry through the IEA’s Industry Advisory Board (IAB), the coal industry through the Coal Industry Advisory Board (CIAB) and the renewable industry through the Renewable Industry Advisory Board (RIAB)
Lead high-level missions to member and partner countries, engaging Ministers and senior policy makers
Lead and develop a Directorate, of over 110 staff (analysts, statisticians, support and consultants) through merit-based recruitment, professional development, and performance management

What we offer

Monthly base salary starting from 16 090 EUR plus allowances, based on eligibility, exempt of French income tax

Fulltime

!

Vice President, Biostatistics

The Vice President, Biostatistics is a key enterprise leader responsible for set...

Location

United States , Philadelphia

Salary:

Not provided

Cabaletta Bio Inc

Expiration Date

Until further notice

Requirements

PhD or Master’s degree in Biostatistics, Statistics, or related field
10+ years of relevant experience in biotech/pharmaceutical R&D, including leadership of statistical strategy for early and late-stage clinical programs
At least 7 years leading Biostatistics teams, including management of statisticians, programmers, and/or data management groups
Demonstrated success in shaping statistical strategy for pivotal trials and regulatory submissions
Proven ability to influence senior stakeholders, navigate ambiguity, and drive alignment across cross-functional teams
Strong track record of contributing to late-stage development/regulatory submissions with BLA experience strongly preferred
Deep understanding of global regulatory guidelines, data requirements, clinical operations interfaces, and inspection readiness
Exceptional communication skills with ability to translate complex statistical concepts into clear, actionable insights for diverse audiences
Experience managing departmental budgets, vendor relationships, and technical infrastructure
Highly collaborative, with strong interpersonal skills and the ability to build trust across teams

Job Responsibility

Lead and develop the Biostatistics and Data Management functions, developing a long-term vision, operating model, and high-performance culture
Recruit, mentor, and inspire the team to ensure organizational capability scales with the company’s clinical portfolio
Serve as a strategic advisor to executive leadership on statistical risk, trial feasibility, portfolio trade-offs, and data-driven decision making
Provide expert statistical input into clinical development strategy, protocol concepts, study design, and endpoint selection to optimize probability of technical and regulatory success
Drive innovative statistical approaches, adaptive designs, and data-driven methodologies to accelerate development timelines and enhance the robustness of clinical findings
Ensure all statistical strategies align with regulatory expectations and meet the needs of future submissions, inspections, and commercial planning
Oversee development and execution of statistical analysis plans, data review strategies, and inferential methodologies for all clinical studies
Ensure the integrity, quality, reproducibility, and validation of statistical analyses, including submission-ready documentation
Partner cross-functionally with Clinical Development, Clinical Operations, Regulatory Affairs, Medical Affairs, CMC, and other teams to ensure seamless execution and data-driven decision making
Provide statistical leadership for regulatory interactions and submissions, including authoring and reviewing statistical components of BLAs, briefing packages, responses, and advisory committee materials

What we offer

health and retirement
PTO
stock option plans

Biostatistics Senior Associate

Amgen is expanding its global Biostatistics capabilities, with Amgen India (AIN)...

Location

India , Hyderabad

Salary:

Not provided

Amgen

Expiration Date

Until further notice

Requirements

Master’s degree in Statistics/Biostatistics (or related subject with high statistical content) with 2 years post-graduate experience as a statistician in the pharmaceutical industry or medical research
Doctoral degree in Statistics/Biostatistics (or related subject with high statistical content) with 1 year post-graduate experience
Competency in statistical programming (SAS or R)
Experience applying statistical methods in the analysis and conduct of clinical trials
Ability to clearly communicate in English, both written and oral

Job Responsibility

Author and provide statistical contributions to Statistical Analysis Plans (SAPs), Table/Figure/Listing (TFL) shells, randomization specifications, submission data file specifications (SDTM/ADaM), and other key study-related documentation
Conduct and document statistical analyses for clinical trials, including primary and secondary endpoint analyses, exploratory analyses, and dose-level review support
Perform and document quality control (QC) of datasets and outputs to ensure accuracy, consistency, and compliance with CDISC standards
Participate in Clinical Study Team (CST) meetings to provide statistical input and represent Biostatistics
Collaborate with programming colleagues to ensure timely delivery of study outputs
Contribute to clinical publications, study reports, and regulatory submissions
Support the review of deliverables from external suppliers for quality
Stay abreast of new methodologies, tools, and regulatory guidelines in statistical practice
Ensure that statistical sections of the Trial Master File (TMF) are maintained and up to date
Adhere to Amgen’s policies, SOPs, and relevant controlled documents, and support audits as needed

What we offer

Vast opportunities to learn and develop within our global organization
Diverse and inclusive community of belonging, where teammates are empowered to bring ideas to the table and act
Generous Total Rewards Plan comprising health, finance and wealth, work/life balance, and career benefits

Senior Statistician

UC San Diego

Location:
United States , La Jolla

Category:
Research and Development

Contract Type:
Not provided

Salary:

Job Description:

Job Responsibility:

Requirements:

Nice to have:

Additional Information:

Job Posted:
March 04, 2026

Expiration:
March 10, 2026

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