Head of Biostatistics Job at Life Science Talent (Søborg)

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

Quality Manager

The job was opened specifically for the support of Biostatistics and Programming...

Location

India

Salary:

Not provided

Parexel

Expiration Date

Until further notice

Requirements

8-12 years’ experience in clinical research
Demonstrated experience in Quality or Risk Management activities
Expertise in root cause methodologies and CAPA development
Proven leadership in mentoring teams and managing complex, multi-project accounts
Comprehensive mastery of ICH-GCP principles and their strategic application
Fluency in written and oral English
Bachelor’s Degree required preferably in life sciences or health-related discipline or equivalent experience
Advanced degree (master’s degree) in a science, technology or industry-related discipline strongly preferred

Job Responsibility

Quality Event support (Quality Rep role)
audit support
Quality support and consultancy generally worldwide but in particular for the India Biostatistics and Statistical Programming teams
partnering with the India heads of these teams
Support of functional SOP updates
participation in general Quality-related initiatives

Director Data Science

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 and 10 years of Scientific and/or work-related experience
Master’s degree and 18 years of Scientific and/or work-related experience
Bachelor’s degree and 20 years of Scientific and/or work-related experience
MS or PhD in Data Science, Computer Science, Informatics, Statistics, Mathematics, Life Sciences, or similar field
10+ years of experience in clinical research and/or predictive analytics
Wide experience analyzing clinical trial, real world, and/or ‘omics data
Specialization in few ML areas ( NLP, Vision, Bayesian Modelling) and provide mentorship to different groups
Led big projects in previous or current roles
Experience of working with Senior Leadership

Job Responsibility

Collaborate with Sr. Directors Data Science/Engineering to set the technical vision, mission, and strategy for the CfDA Data Science group
Continually assess and introduce cutting-edge technologies, ideas, and state-of-the-art ML/AI methodologies for clinical development
Lead the execution of major data science projects, providing technical guidance and ensuring high-quality deliverables
Run cross functional project teams and delivers project end to end
Mentor and guide a team of data scientists, fostering technical growth and expertise
Collaborate closely with IS/other analytical organizations to ensure alignment on analytical platforms and data strategies
Coordinate with Data Science Head to help set vision, mission, and strategy for CfDA Data Sciences group
Identify high-value projects across Clinical Development
Advise Data Science Head during prioritization, resource, and funding decisions
Establish annual goals for CfDA Data Scientists

What we offer

Vast opportunities to learn and move up and across 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

Director, Design & Innovation

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 or higher in Statistics, Biostatistics, Computer Science, Mathematics, Life Sciences, or related scientific discipline
At least 8 years of experience in the pharmaceutical, biotechnology, or medical research industry
Demonstrated experience in people management, including direct reports
Strong written and verbal English communication skills
Experience working effectively in a globally distributed, cross-cultural environment

Job Responsibility

Provides leadership for Design & Innovation functions based in India, ensuring delivery of high-quality, compliant, and value-added outputs aligned with global standards and strategy
Serves as the primary people leader and managerial owner for India-based staff across BMDS, CSM, SS, and GRB
Acts as a strategic partner to global Design & Innovation leaders, supporting execution of the global vision while representing India capabilities, capacity, and growth opportunities
Drives adoption of innovative design, statistical, data stewardship, centralized statistical monitoring, safety monitoring, and randomization/blinding approaches in collaboration with global function heads
Ensures consistent application of Amgen policies, SOPs, and controlled documents across all India-based Design & Innovation activities
Supports capability development, talent pipeline growth, and succession planning for Design & Innovation functions in India
Provides oversight of resourcing, prioritization, and workload balancing across India-based teams
Translate global Design & Innovation strategy into executable plans for India-based teams
Support delivery of innovative statistical methodologies, data standards, centralized statistical monitoring, safety monitoring, and randomization/blinding services
Partner with global leaders to identify opportunities for expanding Design & Innovation capabilities and scope at AIN

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

Sr. Manager/AD, Statistical Programmer

Beam is looking for an associate Director/Director of statistical programming to...

Location

United States , Cambridge

Salary:

155000.00 - 225000.00 USD / Year

Beam Therapeutics

Expiration Date

Until further notice

Requirements

MS or higher degree in Statistics, Mathematics, or related scientific Discipline
At least 12 years Pharmaceutical/Biotech programming experience
Advanced SAS programming skills and strong Statistical background along with experience with SAS Base, SAS/Macros, SAS/Graph and SAS/Stat
Experience and in-depth knowledge in CDISC including STDM, ADaM and controlled terminologies
NDA or BLA submission experience is required
Excellent organizational skills and ability to prioritize tasks
Excellent communication and interpersonal skills
Experience managing CROs and other data vendors
Knowledge of ICH guidelines, Good Clinical Practices, FDA / EMA / other regulatory authority guidance

Job Responsibility

Lead and manage statistical programming activities on clinical studies and oversee CROs to generate analysis data sets and tables, listings and figures needed for clinical study reports and regulatory submissions
Review and validate SDTM, ADaM analysis datasets and TFLs created by CROs
Work collaboratively and communicate effectively with Biostatistics, Data Management, clinical operations, clinical development, Regulatory and other functions
Manage creating CDSIC SDTM and ADaM datasets, analysis metadata results and Define.xml for Electronic Submission from the clinical database or external data sources
Manage the activities of data summary, statistical analysis, patient profile, safety and efficacy tables, listings and figures using Base SAS, SAS Macros, SAS/STAT, SAS/Graph, SAS/SQL, SAS/ODS and R
Oversee and manage the workflow of generating study specific and ad-hoc clinical data listings, summary tables and figures
Partner with Statisticians and other members of the clinical study team, perform ad hoc analysis
Review SAP, DMP, CRF, annotated CRF, TFL specifications and other relevant documents by CROs and provide expert feedback from functional perspective
Assist the Head of Statistical Programming in reviewing bid proposals, monitoring and tracking budgets for outsourced activities
Assist the Head of Statistical Programming to develop and implement programming processes, programming standards and SOPs

Fulltime

Head of RTSM (Randomization and Trial Supply Management)

You will lead the RTSM (Randomization and Trial Supply Management) function in t...

Location

United States;United Kingdom , Collegeville;Stevenage

Salary:

Not provided

GSK

Expiration Date

Until further notice

Requirements

Bachelor's degree in life sciences, pharmacy, engineering, IT, or related field, or equivalent experience
8+ years of experience managing RTSM, IRT, or clinical supply systems in the pharmaceutical or biotech industry
Experience leading cross-functional teams and managing external vendor relationships
Experience with clinical trial operations, randomization methods, blinding and investigational product supply principles
Experience with system vendor selection, implementation, validation, and change control

Job Responsibility

Lead design and delivery of RTSM strategies across Phase I–IV clinical programs and investigator-sponsored studies
Direct cross-functional teams and vendors to ensure on-time randomization, kit assignment, and clinical supply availability to sites and patients
Own risk assessments and contingency plans for trial supply and randomization activities
Establish and improve RTSM processes, metrics, and governance to drive quality and efficiency
Partner with clinical operations, biostatistics, data management, and regulatory functions to align RTSM with study design and compliance needs
Hire, coach and develop a diverse team, and foster collaboration across internal and external partners

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

New

Senior Salesforce Developer

Location

India , Bengaluru

Salary:

Not provided

NTT DATA

Expiration Date

Until further notice

Requirements

Minimum 5–8 years of IT experience, with 4+ years on the Salesforce platform
Strong hands-on experience in Salesforce production support and incident management
Good understanding of Salesforce architecture, data model, and platform features
Hands-on experience with Apex, Lightning Web Components (LWC), Flows, and integrations
Familiarity with ITIL processes (Incident, Problem, Change Management)
Experience with deployment tools (Copado, Gearset, Jenkins, etc.) is a plus
Ability to work with SLAs, prioritize tasks, and manage multiple incidents effectively
Strong analytical and troubleshooting skills
Good communication skills and ability to work with distributed/onshore-offshore teams
Experience working in Agile environments

Job Responsibility

Provide hands-on Salesforce production support, ensuring system availability, stability, and performance across Sales Cloud, Service Cloud, and Experience Cloud
Monitor and triage incidents, perform root cause analysis, and resolve issues within defined SLAs
Work on bug fixes, minor enhancements, and data corrections in production environments
Collaborate with onshore leads, product owners, and engineering teams to prioritize and resolve production issues
Participate in incident management, problem management, and change management processes
Support deployment activities, including validations, smoke testing, and post-release monitoring
Analyze recurring issues and contribute to continuous improvement initiatives and automation opportunities
Ensure proper documentation of incidents, fixes, and known errors in knowledge repositories
Coordinate with cross-functional teams (integration, data, infrastructure) to troubleshoot and resolve issues
Support monitoring, alerting, and system health checks across Salesforce environments

New

Secondary Teaching Assistant

Robert Barclay Academy is looking to appoint a dedicated Teaching Assistant. In ...

Location

United Kingdom , Hoddesdon

Salary:

16700.00 GBP / Year

Scholars' Education Trust

Expiration Date

June 05, 2026

Requirements

Excellent communication skills
Show intuition within a range of everyday task and activities
Want to support the needs of the pupils with flair
'Can do' attitude

Job Responsibility

Support the needs of the pupils

What we offer

High level of training offered within the Academy and Trust at any stage of your career
Opportunities for graduates to progress into Teacher Training Programme
Seeing and being part of pupil’s development and achievements
School place for a child of a permanent member of staff, providing the criteria is met

Parttime

Select Country

Head of Biostatistics

Job Description

Job Responsibility

Requirements

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