CrawlJobs Logo

Senior Medical Statistician

mtmpetcare.com Logo

MTM Pet Care (LECVNG)

Location Icon

Location:

Category Icon

Job Type Icon

Contract Type:
Not provided

Salary Icon

Salary:

Not provided

Job Description:

Does supporting world-class research and improving lives of patients excite you? Our dynamic and internationally recognised research company Observation & Pragmatic Research Institute, (OPRI) is looking for a highly motivated and dynamic member for our statistics team. The role can be based in one of our Singapore, Cambridge or Brisbane offices. For experienced individuals, remote working may also be considered. The successful candidate will work within a multidisciplinary team consisting of researchers, epidemiologists, medical experts, medical writers and other statisticians. This is a fantastic opportunity to work with large-scale electronic health record databases, patient registries and conduct pragmatic clinical studies across a range of therapeutic areas.

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
  • Mentor junior researchers

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

Additional Information:

Job Posted:
December 10, 2025

Work Type:
On-site work
Job Link Share:

Looking for more opportunities? Search for other job offers that match your skills and interests.

Briefcase Icon

Similar Jobs for Senior Medical Statistician

Vice president global head of statistics vcrd

Pfizer is seeking a Vice President, Global Head of Statistics to join our thrivi...
Location
Location
United States , Pearl River; Collegeville
Salary
Salary:
274000.00 - 426800.00 USD / Year
pfizer.de Logo
Pfizer
Expiration Date
Until further notice
Flip Icon
Requirements
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
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
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
Read More
Arrow Right

Biostatistician II

We are seeking a skilled and motivated Biostatistician II to join our fast-paced...
Location
Location
United States of America
Salary
Salary:
100000.00 - 120000.00 USD / Year
canfieldsci.com Logo
canfield scientific
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Master’s degree in Biostatistics, Statistics, Mathematics, or a related quantitative discipline
  • 3–5 years of experience in clinical research within a regulated environment including contributing to Statistical Analysis Plans (SAPs) and drafting sections under senior statistical oversight
  • Demonstrated proficiency in SAS, including development of validated analysis programs and implementation of standard QC procedures
  • Solid understanding of statistical methodology for clinical trials, including analysis population definitions, common endpoint types, handling of missing data, and basic multiplicity considerations
  • Working knowledge of ICH E9/E9(R1) principles and general FDA regulatory expectations
  • Ability to implement predefined analyses independently and contribute to statistical design discussions with appropriate supervision and manage assigned studies or analysis workstreams within established timelines
  • Experience contributing to statistical sections of CSRs, TLF specifications, and other regulatory-facing documents
Job Responsibility
Job Responsibility
  • Contribute to the development and authoring of Statistical Analysis Plans (SAPs), including drafting key sections (analysis populations, endpoints, missing data handling, sensitivity analyses) under senior statistical guidance
  • Support protocol development through input on endpoint definitions, statistical methodology, and sample size considerations
  • Independently develop, validate, and maintain statistical programs for assigned analyses in SAS
  • Participate in data review activities, and perform data quality checks in collaboration with data management
  • Perform and interpret statistical analyses aligned with study objectives and regulatory requirements
  • Draft statistical sections of clinical study reports, TLF shells, and other regulatory-facing documents, with review from senior statisticians
  • Ensure analyses adhere to ICH and FDA guidance, following established departmental standards and QC procedures
  • Collaborate cross-functionally with clinical, regulatory, data management, and medical writing teams to support study deliverables
  • Contribute to process improvement, template development, and standardization initiatives
What we offer
What we offer
  • Paid days off
  • Medical, dental, and vision insurance
  • May be eligible for a discretionary bonus
  • 401(k) plan with employer match (currently set at 50%)
  • Fulltime
Read More
Arrow Right
New

Principal Statistician - Medical & Market Access Statistics

GSK Oncology has a commitment to the discovery and development of new oncology t...
Location
Location
United Kingdom; United States , Stevenage; London; Collegeville; Waltham
Salary
Salary:
126225.00 - 210375.00 USD / Year
us.gsk.com Logo
GSK
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • MSc or PhD in Statistics, Mathematics or equivalent with relevant experience in clinical research, pharmaceutical, CRO, or academic settings
  • Proven statistical contributions and accomplishments in late-phase clinical drug development
  • Good statistics programming skills and experience in R and/or python
  • Self-motivated with strong time management skills to manage multiple tasks effectively across projects
  • Excellent interpersonal and communication skills, including the ability to explain methods to senior stakeholders, and ability to build and maintain strong working relationships
  • Experience successfully influencing across functions and organizational levels
Job Responsibility
Job Responsibility
  • Provide statistical input for the design, analysis, reporting, and interpretation of non-registrational studies
  • Shape clinical development plans, HTA strategies, and commercial approaches
  • Build and maintain strategic relationships with internal and external stakeholders to address business needs
  • Develop and implement novel statistical methods to tackle complex challenges
  • Address market access and reimbursement challenges from regional agencies by collaborating with cross-functional teams
  • Work with Health Outcomes and Market Access teams to analyze and interpret clinical trials and real-world data, while expanding expertise beyond traditional statistics
What we offer
What we offer
  • Competitive base salary
  • Annual bonus based on company performance
  • Flexible working options
  • Learning and career development
  • Access to healthcare & wellbeing programmes
  • Employee recognition programmes
  • Pension plan membership
  • Shares and savings programme
  • Fulltime
Read More
Arrow Right

Principal Statistician

The Principal Statistician will provide senior-level statistical expertise to su...
Location
Location
United Kingdom
Salary
Salary:
Not provided
gt-hq.com Logo
GT
Expiration Date
Until further notice
Flip Icon
Requirements
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
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
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
Read More
Arrow Right

Senior Manager Biostatistics (Study Lead Statistician)

How might you defy imagination? If you feel like you're part of something bigger...
Location
Location
India , Hyderabad
Salary
Salary:
Not provided
amgen.com Logo
Amgen
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Doctorate degree in Statistics/Biostatistics or related subject with high statistical content and at least 6 years of post-graduate statistical experience in the pharmaceutical industry or medical research
  • Master's 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
  • Bachelor'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
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
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
  • Fulltime
Read More
Arrow Right

Biostatistics Senior Associate

Amgen is expanding its global Biostatistics capabilities, with Amgen India (AIN)...
Location
Location
India , Hyderabad
Salary
Salary:
Not provided
amgen.com Logo
Amgen
Expiration Date
Until further notice
Flip Icon
Requirements
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
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
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
Read More
Arrow Right

Vice President, Biostatistics

The Vice President, Biostatistics is a key enterprise leader responsible for set...
Location
Location
United States , Philadelphia
Salary
Salary:
Not provided
cabalettabio.com Logo
Cabaletta Bio Inc
Expiration Date
Until further notice
Flip Icon
Requirements
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
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
What we offer
  • health and retirement
  • PTO
  • stock option plans
Read More
Arrow Right

Senior Manager Biostatistics

Amgen is expanding its global Biostatistics capabilities, with Amgen India (AIN)...
Location
Location
India , Hyderabad
Salary
Salary:
Not provided
amgen.com Logo
Amgen
Expiration Date
Until further notice
Flip Icon
Requirements
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
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
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
Read More
Arrow Right