Senior Medical Statistician Job at MTM Pet Care (LECVNG)

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

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

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

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

Senior Manager Biostatistics

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

Location

India , Hyderabad

Salary:

Not provided

Amgen

Expiration Date

Until further notice

Requirements

Doctorate degree in Statistics/Biostatistics or related subject with high statistical content and at least 8 years of post-graduate statistical experience in the pharmaceutical industry or medical research
Or Master’s degree in Statistics/Biostatistics or related subject with high statistical content and at least 12 years of post-graduate statistical experience in the pharmaceutical industry or medical research

Job Responsibility

Utilizing knowledge and expertise to inform and provide sound statistical guidance to areas and teams in clinical development, reimbursement, and medical affairs.
Plan and execute statistical contributions to protocols, Flash Memos and Clinical Study Reports (CSRs)
Implement, manage and support standards, technical quality and consistent approaches in strategy, study design and statistical analysis.
Knowledgeable of developments in the field of statistics in drug development (innovative trial design) and Amgen’s statistical policies, procedures and strategies.
Understand, promote, and communicate innovative and standard statistical methodologies, trial design, data analysis, and medical / clinical understanding for product
Oversee statistical contributions to key design elements, protocols, randomization specifications, statistical analysis plans, tables, figures and listing shells, submission data file specifications, and other key study-related documentation
Collaborate cross-functionally to deliver robust, valid and scientifically rigorous analysis results in Table, Figure and Listings (TFLs), Flash Memos (FM), Clinical Study Reports (CSRs), clinical publications, and other communications
Serve as the GBS lead on the Clinical Study Team leadership team to execute clinical trials according to the protocol, performing risk assessments and ensuring quality data collection and alignment between data collection and study objectives
Contribute to clinical publications, regulatory filing documents, reimbursement documents and other communications for product or study
Provide statistical consultancy, training, and advice within Amgen

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 Biostatistician

Job opportunity for a permanent, onsite Senior Biostatistician role in Paris, Fr...

Location

France , Paris

Salary:

Not provided

AB SCIENCE

Expiration Date

Until further notice

Requirements

Ph.D. in Statistics with minimum 3 years of relevant pharmaceutical (or CRO) industry work experience or Masters in Statistics or equivalent with minimum 5 relevant pharmaceutical (or CRO) industry work experience
Good Knowledge of SAS
Good Understanding of CDISC Concepts
Good understanding of ICH guidelines
Fluent in English

Job Responsibility

Author the Statistical Sections of Protocol
Propose and Review the Study design
Calculate the sample size
Review the Case Report Form (CRF)
Review the Edit Check Document (specifically for critical modules like RECIST 1.1 etc.)
Write the randomization specifications and coordinate and finalize all the randomization activities with the IWRS vendor
Author Statistical Analysis Plan (interim and final as appropriate)
Perform the Statistical Analysis (Efficacy and Safety (key safety like Adverse Events)) using SAS
Ensure quality of all the outputs developed
Perform the role of validator as appropriate

What we offer

Permanent position
Salary & package to define according skills and experience

Fulltime

New

Youth Behavior Mentor

You’ll be joining a specialist alternative provision school in Bristol that give...

Location

United Kingdom , Bristol

Salary:

Not provided

AFFINITY WORKFORCE

Expiration Date

Until further notice

Requirements

Experience supporting young people with behaviour needs, SEMH or complex backgrounds
A full UK driving licence and access to a vehicle, as outreach is part of the role

Job Responsibility

Mentoring young people with behavioural, emotional and social needs
Being a calm and steady presence when pupils face challenging moments
Offering outreach support for students struggling to attend or engage
Helping young people regulate, reset and return to learning
Working closely with pastoral and safeguarding teams to embed personalised behaviour plans
Encouraging pupils to grow emotionally, build resilience and develop positive routines
Providing consistent support that helps pupils feel seen, heard and believed in

What we offer

A supportive, friendly and collaborative school team
Training, development and opportunities to grow your skills
A chance to make a meaningful, lifelong impact on a young person’s journey

Fulltime

New

Postdoctoral Research Associate

The Faculty of Humanities and Social Sciences, at Birkbeck, University of London...

Location

United Kingdom , London

Salary:

22124.00 - 25189.00 GBP / Year

Birkbeck University of London

Expiration Date

May 18, 2026

Requirements

Strong foundation in early modern studies
Good first degree in a relevant subject (e.g. English Literature, History)
Completed PhD in a related discipline
Record of academic publication supported by clear plans for future research - or equivalent experience
Basic ability to work with databases and to research English-language manuscript and print materials from c.1570–1730
Willingness to further develop these skills
Ability to write to a high academic standard
Ability to manage time effectively, prioritise tasks, and meet deadlines

Job Responsibility

Carry out dedicated research on non‑elite textual production
Work extensively with manuscripts and printed sources
Visit archives
Investigate datasets
Develop the project database
Contribute to shaping the project’s scholarly outputs
May be involved in textual editing
Focus on one of two thematic strands: Non‑elite writing produced in the provinces, or Writing produced by non‑elite women
Identify and analyse sources
Explore methodological approaches that bring together literary and historical perspectives

What we offer

Competitive salary and pension scheme
31 days paid leave
Flexible working arrangements
Generous benefits in the HE sector
Located in the heart of Bloomsbury, Euston, London

Parttime

Senior Medical Statistician

MTM Pet Care (LECVNG)

Location:

Category:
Research and Development

Contract Type:
Not provided

Salary:

Job Description:

Job Responsibility:

Requirements:

Additional Information:

Job Posted:
December 10, 2025

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