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Biotech jobs in United Kingdom

Statistician

F. Hoffmann-La Roche AG

United Kingdom
On-site
GBP 45,000 - 65,000
30+ days ago
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(Senior) Director, Clinical Operations

BioNTech

City of London
On-site
GBP 125,000 - 150,000
30+ days ago

Director Global Regulatory Affairs

BioNTech

City of London
On-site
GBP 60,000 - 80,000
30+ days ago

Customer Success Manager

Latent Labs Ltd.

City of London
On-site
GBP 80,000 - 100,000
30+ days ago

Senior Director, Statistical Programming

BioNTech

City of London
On-site
GBP 197,000 - 240,000
30+ days ago
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Senior Manager, Global Marketing Development (Clinical Research)

Thermo Fisher Scientific Inc.

Birmingham
On-site
GBP 60,000 - 80,000
30+ days ago

Assistant Animal Technician 1

Charles River

United Kingdom
On-site
GBP 40,000 - 60,000
30+ days ago

Competitive & Portfolio Intelligence Lead

Methodfi

City of London
On-site
GBP 60,000 - 80,000
30+ days ago
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Associate Director, Country Clinical Operations, UK

BioNTech

City of London
On-site
GBP 70,000 - 90,000
30+ days ago

Senior Microsoft 365 Administrator

Pharmaron Beijing Co. Ltd.

United Kingdom
On-site
GBP 60,000 - 80,000
30+ days ago

Senior Project Associate

ICON plc

United Kingdom
On-site
GBP 100,000 - 125,000
30+ days ago

EMEA Trade Compliance Leader — Digital Transformation

Moderna Therapeutics

City of London
On-site
GBP 80,000 - 100,000
30+ days ago

Global Regulatory Lead, Oncology Strategy & Dossiers

BioNTech

City of London
Hybrid
GBP 60,000 - 80,000
30+ days ago

Director, European Regulatory Policy & R&D Strategy

Amgen Inc

Uxbridge
Hybrid
GBP 90,000 - 120,000
30+ days ago

UK Head of Clinical Operations - Lead UK Trials Network

BioNTech

City of London
On-site
GBP 125,000 - 150,000
30+ days ago

Oncology Translational Leader – Biomarker Strategy

BioNTech

City of London
On-site
GBP 100,000 - 125,000
30+ days ago

Senior Director, Statistical Programming — Global Submissions & AI/ML

BioNTech

City of London
On-site
GBP 197,000 - 240,000
30+ days ago

Biotech Data Engineer: ML Pipelines & DataOps

Methodfi

City of London
On-site
GBP 55,000 - 75,000
30+ days ago

UK Clinical Operations Lead - Trials Delivery

BioNTech

City of London
On-site
GBP 70,000 - 90,000
30+ days ago

Associate Account Director - Advertising

Syneos Health

City of London
On-site
GBP 65,000 - 85,000
30+ days ago

Clinical Trial Manager (Associate Director) - Stirling

Medpace Inc.

Stirling
Remote
GBP 60,000 - 80,000
30+ days ago

Executive Director, Global Product Strategy: GI/GU & Early Assets

BioNTech

City of London
Hybrid
GBP 125,000 - 150,000
30+ days ago

Global Oncology Product Strategy Lead (GI/GU)

BioNTech

City of London
Hybrid
GBP 125,000 - 150,000
30+ days ago

Graduate Electronics Engineer

Amododesign

Sheffield
On-site
GBP 80,000 - 100,000
30+ days ago

Senior Firmware Engineer

Amododesign

Sheffield
On-site
GBP 125,000 - 150,000
30+ days ago

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Statistician
F. Hoffmann-La Roche AG
United Kingdom
On-site
GBP 45,000 - 65,000
Full time
30+ days ago

Job summary

A global healthcare company in Welwyn is seeking a Statistician to contribute statistical expertise in clinical trial design and analysis. The ideal candidate will hold an MSc or PhD in a related quantitative field and possess experience in clinical trial statistics within a pharmaceutical environment. This position offers an opportunity to drive scientific rigor in clinical development and ensure compliance with regulations, making a significant impact on patient healthcare solutions.

Qualifications

  • Experience in clinical trial statistics within pharma, biotech, or CRO.
  • Familiarity with ICH guidelines and regulatory requirements.
  • Capacity for independent thinking and strategic agility.

Responsibilities

  • Apply statistical expertise to clinical trial design and analysis.
  • Draft and review statistical analysis plans and protocols.
  • Support statistical analyses and address complex data issues.

Skills

Clinical trial statistics
Statistical principles
Independent decision-making
SAS and/or R proficiency
Excellent communication skills

Education

MSc or PhD in Statistics or related field

Tools

SAS
R
Job description
Statistician page is loaded## Statisticianlocations: Welwyntime type: Full timeposted on: Posted Todayjob requisition id: 202511-128866At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.### ### The PositionA healthier future. It’s what drives us to innovate. To continuously advance science and ensure everyone has access to the healthcare they need today and for generations to come. Creating a world where we all have more time with the people we love. That’s what makes us Roche.This role is within Biostatistics, a core function within Product Development Data Science and Analytics (PDD) that provides strategic leadership and scientific rigor across Development at Roche. Biostatistics identifies opportunities to apply the full breadth of data, digital, and design capabilities to deploy innovative methods across PDD, PD and the broader Roche Pharma organization.As trusted analytical partners in end-to-end drug development, Biostatistics leverages data to drive scientifically rigorous programmatic decisions across Roche’s Development portfolio; Biostatistics designs robust trials and analysis plans that increase the probability of technical success, accelerating timelines to advance Roche’s clinical pipeline and promote regulatory success — ultimately bringing medicines to our patients faster.**The Opportunity:**The **Statistician**is a key member of the cross-functional study or molecule team, responsible for applying statistical expertise to the design, conduct, analysis, and interpretation of individual clinical trials. This role ensures the scientific rigor and regulatory compliance of the study by contributing to protocol development, authoring statistical analysis plans, performing or overseeing data analyses, and supporting the interpretation and communication of results. The Statistician plays a critical role in ensuring that each study generates robust, meaningful data to support decision-making and regulatory submissions.* You contribute to trial design under guidance, applying standard statistical methods* You draft and review protocols, statistical analysis plans (SAPs), and case report forms (CRFs) using templates and precedents* You perform or support statistical analyses as per statistical analysis plans, escalating issues when needed* You represent Biostatistics and PDD at the Study Team level, ensuring statistical and scientific rigor of study deliverables under guidance* You collaborate with study team members to meet deliverables, following existing processes* You summarize findings clearly with support from senior colleagues* You contribute to CSR development and regulatory responses using established templates* You apply judgment to address moderately complex statistical or data issues, balancing scientific rigor with appropriate flexibility, and seek guidance when facing novel or ambiguous situations* You adhere to functional standards by participating in peer review and mentoring relationships to uphold quality and build methodological and regulatory expertise**Who You Are:*** You hold an MSc or PhD in Statistics, Biostatistics, or a closely related quantitative field* You have experience in clinical trial statistics within a pharmaceutical, biotech, or CRO setting* You are familiar with ICH guidelines, GCP, and regulatory requirements (e.g., FDA, EMA)* You have a strong understanding of statistical principles and methodology relevant to clinical trial design and analysis* You are proficient in SAS and/or R and familiar with CDISC standards* You demonstrate capacity for independent thinking and ability to make decisions based upon sound principles* You bring excellent strategic agility including problem-solving and critical thinking skills, and agility that extends beyond the technical domain* You demonstrate respect for cultural differences when interacting with colleagues in the global workplace* You have excellent verbal and written communication skills, specifically in the areas of presentation and writing, with the ability to explain complex technical concepts in clear languagePreferred:* Experience working in cross-functional teams* Effective communication skills with the ability to translate complex statistical concepts for non-statistical audiences* Experience with multiple phases of drug development (early and/or late stage)* Excellent communication skills, including the ability to influence and translate complex data for non-technical stakeholders* Strategic mindset with the ability to contribute to portfolio-level decisionsLocation* This position is based in Welwyn* Relocation Assistance is not available#PDDUK# Who we areA healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.Let’s build a healthier future, together.The statements herein are intended to describe the general nature and level of work being performed by employees, and are not to be construed as an exhaustive list of responsibilities, duties, and skills required of personnel so classified. Furthermore, they do not establish a contract for employment and are subject to change at the discretion of Roche Products Ltd. At Roche Products we believe diversity drives innovation and we are committed to building a diverse and flexible working environment. All qualified applicants will receive consideration for employment without regard to race, religion or belief, sex, gender reassignment, sexual orientation, marriage and civil partnership, pregnancy and maternity, disability or age. We recognise the importance of flexible working and will review all applicants’ requests with care. At Roche difference is valued and we are proud to be an equal opportunity employer where you are encouraged to bring your whole self to work.
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* The salary benchmark is based on the target salaries of market leaders in their relevant sectors. It is intended to serve as a guide to help Premium Members assess open positions and to help in salary negotiations. The salary benchmark is not provided directly by the company, which could be significantly higher or lower.

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