Principal

• Lead statistics for individual studies, related studies, integrated summaries, and regulatory filings
• Design and report Phase I to IV clinical studies
• Provide statistical expertise to clinical development projects
• Develop and execute statistical strategy, study designs, and clinical-trial analyses
• Collaborate with clinical development, pharmacology, pharmacovigilance, clinical drug supply, project management, regulatory affairs, medical writing, clinical data management, and clinical operations
• Manage work performed by external statistics and programming vendors
• Participate in department and cross-functional meetings to optimize study designs, endpoints, and analysis strategies
• Support development and implementation of study protocols
• Review and help validate data capture systems
• Develop statistical programs for clinical-trial simulations, analyses, data displays, and validation
• Write and review statistical analysis plans
• Perform and oversee data analysis and validation, and interpret analyses
• Prepare for and attend regulatory-agency meetings
• Develop, implement, and maintain department standards and practices
• Review CRO timelines and analysis plans for timeliness and quality
• Review and validate CRO deliverables
• Act as statistical subject matter expert for clinical reports, integrated summaries, and other documents
• Respond to statistical questions from regulatory agencies

Senior Principal Statistician, Biostatistics

• Develop compelling stories, impactful campaigns and conceptual design solutions
• Lead complex projects and define creative direction
• Identify opportunities for growth and add value to clients, projects and the business
• Lead pitches, present ideas and build trust with clients and stakeholders
• Collaborate with Principals, the leadership team, digital teams and business leaders
• Mentor and develop team members at all levels
• Direct and motivate multidisciplinary teams
• Meet clients to discuss goals for campaigns and projects
• Develop marketing strategies aligned with company goals
• Create documentation and project briefs
• Track, adjust or end marketing strategies based on results
• Contribute to business development and develop the future work pipeline
• Champion continuous improvement, knowledge sharing and creative ambition

Principal Creative

• Provide technical advice and expertise on technology projects
• Support development of information rights policy
• Support supervisory functions relating to qualified trust services under UK eIDAS
• Contribute technical expertise to digital identity, authentication, trust services, digital credentials and associated technologies
• Support technical assessments, investigations, research activities and regulatory projects relating to online trust
• Participate in assessments of trust service providers and related regulatory and technical evaluations
• Build relationships within the ICO and translate technical insights into regulatory and policy outcomes
• Provide strategic advice through briefings, analysis and recommendations
• Monitor developments in online trust and implications for information rights, including standards, interoperability, privacy, security, fraud prevention, usability and inclusion
• Develop relationships with stakeholders across government, industry, academia and standards bodies
• Represent the ICO in technical discussions, conferences, workshops and meetings
• Contribute to organisational capability in identity, trust and emerging technologies
• Undertake structured learning, professional development and specialist technical training

Principal Technology Adviser – Identity and Trust

• Lead and deliver complex ecological surveys, assessments, and mitigation across development, infrastructure, conservation, and biodiversity enhancement projects
• Provide technical expertise
• Manage projects and client relationships
• Mentor junior staff
• Conduct Preliminary Ecological Appraisals (PEAs)
• Conduct protected species surveys, including bats, GCN, reptiles, and badgers
• Prepare ecological reports, including Ecological Impact Assessments (EcIA), Biodiversity Net Gain (BNG) assessments, and mitigation plans
• Ensure compliance with relevant legislation, planning policy, and best practice guidance
• Liaise with clients, planning authorities, conservation bodies, and other stakeholders

Senior/Principal Ecologist

• Analyse wastewater catchment performance
• Model scenarios and propose and review technical solutions
• Monitor intervention performance
• Contribute to the technical design and assurance of the storm overflow programme
• Provide technical input, options, challenge, steer and governance for AMP8 interventions
• Undertake technical assurance of storm overflow programme benefits
• Design monitoring programmes and conduct modelling and analysis
• Measure intervention benefits and support justification of PR24 assumptions for approximately £2 billion investment
• Support innovative analytical approaches with the Technical Lead and thought leaders across Southern Water, academia, the UK water industry and supply chain
• At Principal level, provide technical authority, guide programme direction and influence decisions
• At Specialist level, contribute wastewater engineering/modelling expertise

Wastewater Networks Technical Specialist – Principal

• Support the design and reporting of Phase I to IV clinical studies
• Support regulatory filings under the supervision of a more senior statistician
• Lead statistical aspects of study design, analysis, validation, and documentation
• Provide statistical expertise for clinical trials, including early-stage trials
• Develop and execute statistical strategy, design, and analyses
• Collaborate with clinical development, pharmacology, pharmacovigilance, clinical drug supply, project management, regulatory affairs, medical writing, clinical data management, and clinical operations
• Oversee statistics and programming work performed by external vendors
• Participate in data science and cross-functional meetings to optimize study designs, endpoints, and analysis strategies
• Support study protocols and review and validate study-specific data capture systems
• Develop statistical programs for clinical trial simulations, analyses, data displays, and validation
• Write statistical analysis plans, perform data analysis and validation, and interpret analyses
• Support the project lead statistician
• Prepare for and attend regulatory agency meetings and respond to statistical questions
• Work closely with statistical programming colleagues
• Monitor CRO guidelines and standards and review and validate CRO deliverables
• Collaborate with medical writers on clinical reports, integrated summaries, and other documents
• Learn and apply drug development regulatory requirements, including CDISC SDTM and ADaM standards
• Stay current with developments in statistics, drug development, and regulatory guidance through literature review, conference attendance, and professional development

Principal Statistician, Biostatistics

• Lead statistical support for the design and reporting of Phase I to IV clinical studies
• Support regulatory filings under the supervision of a more senior statistician
• Manage statistical aspects of study design, analysis, validation, and documentation
• Develop and execute statistical strategy, design, and analyses for clinical trials
• Participate in data science and cross-functional meetings to optimize study designs, endpoints, and analysis strategies
• Collaborate with study teams to meet study and recurring report timelines
• Support development and implementation of study protocols
• Review and validate study-specific data capture systems
• Develop statistical programs to simulate trial design operating characteristics, perform analyses, prepare data displays, and verify data accuracy and validity
• Write statistical analysis plans, perform data analysis and validation, and interpret analyses
• Support the project lead statistician
• Prepare for and attend regulatory agency meetings and respond to statistical questions
• Work closely with statistical programming colleagues
• Monitor CRO guidelines and standards and review and validate CRO deliverables
• Collaborate with medical writers on clinical reports, integrated summaries, and other documents
• Learn and apply drug development regulatory requirements, including statistical contributions to marketing applications and CDISC SDTM and ADaM standards
• Stay current with developments in statistics, drug development, and regulatory guidance

• Execute the field-level alliance motion with select strategic Remote Embedded Partners across UK&I
• Build trust, create demand, and convert ecosystem engagement into sourced and influenced pipeline for Global Payroll, Employer of Record (EOR), and Contractor Management / Contractor of Record (CM/COR)
• Partner with Embedded Sales, Partner Marketing, Sales Enablement, Solutions Consulting, and cross-functional stakeholders
• Build and maintain relationships with Partners’ field stakeholders
• Run account mapping and coverage planning with Partners’ GTM teams
• Embed into Partners’ pipeline reviews, regional meetings, and enablement sessions
• Source opportunities from Partner field teams and related SIs
• Support co-sell execution, including qualification, stakeholder mapping, mutual action plans, and resource coordination
• Report on relationship coverage, sourced/influenced pipeline, conversion, and next steps
• Drive awareness through enablement, content distribution, and local advocacy
• Organize, sponsor, and attend field and ecosystem events
• Own event execution, including targeting, meeting scheduling, on-site engagement, and post-event conversion
• Follow a disciplined weekly operating rhythm
• Capture partner feedback and competitive insights
• Help build and refine alliance playbooks and reusable assets

Strategic Alliances Principal

• Lead and deliver natural capital-focused projects
• Support Biodiversity Net Gain, Nature Positive, Net Zero and Social Value initiatives
• Provide technical leadership and oversight to ensure high-quality outputs meet time, cost and quality requirements
• Lead multidisciplinary project teams and coordinate inputs across AtkinsRéalis
• Apply professional judgement to complex challenges and help clients navigate policy, regulatory and commercial landscapes
• Manage project programmes, budgets and resources
• Build trusted client relationships
• Identify opportunities to deliver additional value through environmental and infrastructure capabilities
• Contribute to and lead proposals and bids
• Help grow the natural capital and environmental economics portfolio
• Shape innovative approaches, methodologies and digital tools
• Coach and mentor junior colleagues
• Contribute to technical networks and capability development activities
• Promote technical excellence internally and externally through clients, industry groups and the wider profession

Principal jobs in United Kingdom

Senior Principal Statistician, Biostatistics

Principal Creative

Principal Technology Adviser – Identity and Trust

Senior/Principal Ecologist

Wastewater Networks Technical Specialist – Principal

Principal Statistician, Biostatistics

Principal Statistician, Biostatistics

Strategic Alliances Principal

Principal – Natural Capital