Last updated: 2025-05-22

30 Clinical Data And Biostatistics jobs in London.

Hiring now: Sr Dir Patient Safety Ris @ Astrazenec, Biostatistics Sr Mgr Hta @ Amgen, Regulatory Data Steward @ Biomarin P, Associate Dir Data Eng Le @ Novartis, Sr Medical Editor @ Ogilvy Hea, Regulatory Affairs Mgr Cm @ Parexel, Associate Dir Clinical Me @ Biomarin, Principal Health Economic @ Putnam An , Statistical Programmer @ Lindus Hea, Lead The Define And Deliv @ Genomics E.Explore more at at kaamvaam.com

🔥 Skills

Clinical Trials (8) Data Management (7) biostatistics (6) clinical trials (6) project management (6) Biostatistics (6) data analysis (5) Statistical Programming (5) cross-functional collaboration (4) Regulatory Affairs (4)

📍 Locations

London (25) High Wycombe (4) Luton (1)

Astrazeneca

Skills & Focus: patient safety, risk management, regulatory strategies, oncology, collaboration, innovation, health authority, training, methodologies, pharmacovigilance
About the Company: AstraZeneca is one of the world’s most forward-thinking and connected BioPharmaceutical companies, dedicated to delivering life-changing medicines.
Experience: Extensive experience in patient safety/pharmacovigilance and risk management, including applicable industry experience.
Salary: Competitive + Excellent Flexible Benefits!
Type: Full-time
Benefits: Excellent Flexible Benefits

Amgen

Skills & Focus: biostatistics, HTA, data analysis, cross-functional collaboration, clinical trial design, statistical expertise, EU HTA regulation, problem-solving, statistical software, policy development
About the Company: Amgen is one of the world's leading biotechnology companies, dedicated to serving patients through global collaboration in research, manufacturing, and deliver…
Experience: Post graduate statistical experience in the biopharmaceutical industry or medical research.
Type: Full time
Benefits: Generous Total Rewards Plan comprising health, finance, and wealth, work/life balance, and career benefits.

Biomarin Pharmaceutical Inc.

Skills & Focus: Regulatory Affairs, data management, Veeva, Pharma, clinical trials, data governance, data quality, Regulatory Master Data, analytical skills, communication skills
About the Company: BioMarin is a global biotechnology company that relentlessly pursues bold science to translate genetic discoveries into new medicines that advance the future o…
Experience: Greater than 5 years of experience in Regulatory Affairs, with 3 years in Regulatory Information Management/Data Stewardship

Novartis

Skills & Focus: data engineering, AI, clinical trials, data pipelines, automation, quantitative science, research and development, data assets, collaboration, software pipelines
About the Company: Novartis is an innovative medicines company focused on reimagining medicine to improve and extend people’s lives. They work to empower patients, healthcare pro…
Type: Full-time

Biomarin Pharmaceutical Inc.

Skills & Focus: Clinical Development, program management, project management, cross-functional leadership, clinical trial delivery, strategic thinking, data analytics, vendor management, team management, change management
About the Company: BioMarin is a global biotechnology company that relentlessly pursues bold science to translate genetic discoveries into new medicines that advance the future o…
Experience: 10+ years clinical trial or drug development experience in biotechnology, pharmaceuticals, medical device organizations

Ogilvy Health

Skills & Focus: medical editing, medical communications, scientific literature, regulatory guidelines, editorial processes, accuracy, clarity, therapeutic areas, interpersonal skills, expertise
About the Company: Ogilvy was founded in 1948 by David Ogilvy. David created a culture that deeply respects and cares about its people and clients. Our mission is to inspire peop…
Experience: Significant experience as a Medical Editor within a medical communications agency.
Type: Fixed-term contract
Benefits: Private Medical Cover OR Monthly Leisure Allowance (£45!) OR Dental Cover, 25 days annual leave, plus a day off for you…

Parexel

Skills & Focus: Regulatory Affairs, Manager, CMC, biologics, clinical trials, consulting, biostatistics, medical writing, health economics, project management
Skills & Focus: Regulatory Affairs, CMC, biologics, Clinical Research, Data Science, Advanced Analytics, Consulting, Clinical Trials, Project Leadership, Biostatistics
About the Company: Parexel provides comprehensive drug development and regulatory consulting services.

Biomarin

Skills & Focus: clinical writing, medical writing, regulatory submissions, clinical development, document management, cross-functional collaboration, vendor management, team leadership, scientific expertise, budgeting
About the Company: BioMarin is a global biotechnology company that relentlessly pursues bold science to translate genetic discoveries into new medicines that advance the future o…
Experience: At least 10 years of experience as a medical writer in the pharmaceutical industry. Minimum of 3 years administrative and/or functional management experience.
Type: Hybrid

Putnam, An Inizio Advisory Company

Skills & Focus: health economic models, HTA, cost-effectiveness, budget impact models, economic modelling, decision analytic modelling, project management, health economics, software packages (e.g., STATA, R), clinical decision-making
About the Company: Putnam is a leading scientific and strategic consulting partner in the life sciences industry, supporting global clients with strategic insights and solutions …
Experience: 7-10 years of experience in economic modelling for health technology assessment (HTA)
Benefits: Participation in international projects, competitive salary, hybrid work model, career development, diverse training, c…

Lindus Health

Skills & Focus: Statistical Programming, Clinical Trials, R Programming, Data Processing, Data Analysis, Data Standards, Regulatory Requirements, Data Manipulation, Reporting, Collaboration
About the Company: Lindus Health aims to modernize the clinical trial process using software to facilitate faster, more reliable, and patient-friendly clinical trials. Since its …
Experience: 3-5 years experience working with clinical trial data
Benefits: Competitive salary, meaningful stock options, unlimited holidays, health insurance, wellness allowance, enhanced parent…

Genomics England

Skills & Focus: scientific research, data analysis, genomics, strategic planning, research data, biobank, governance, compliance, leadership, healthcare

Iqvia

Skills & Focus: biostatistics, consulting, healthcare, statistical analysis, programming, study protocols, data management, collaboration, research, analysis
About the Company: IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industrie…
Type: Full time
Benefits: Benefits programs are designed to meet your total well-being needs so you can thrive at work and at home.

Biomarin Pharmaceutical Inc.

Skills & Focus: Regulatory, Data Steward, Regulatory Information Management, Data Quality, Pharma, Clinical Trials, Veeva, Data Management, Compliance, Documentation
About the Company: BioMarin is a global biotechnology company that relentlessly pursues bold science to translate genetic discoveries into new medicines that advance the future o…
Experience: Greater than 5 years of experience in Regulatory Affairs, with 3 years in Regulatory Information Management/Data Stewardship

Costello Medical

Skills & Focus: statistics, data analysis, clinical trial data, Bayesian analysis, frequentist analysis, R programming, Excel, project management, healthcare, statistical methodologies
About the Company: Costello Medical is a rapidly growing global healthcare agency specialising in medical communications, market access and health economic and outcomes research.…
Experience: Recent graduates and post-graduates, as well as current students.
Salary: £2,150 per month
Type: Full-time, temporary internship
Benefits: Hybrid working options, statutory holiday allowance, flexible working hours, employer pension contributions, as well as…

Biomarin Pharmaceutical Inc.

Skills & Focus: Clinical Development, Drug Development, Clinical Trials, Program Management, Team Management, Collaboration, Communication, Strategy, Stakeholder Engagement, Process Improvement
About the Company: BioMarin is a global biotechnology company that relentlessly pursues bold science to translate genetic discoveries into new medicines that advance the future o…
Experience: 10+ years clinical trial or drug development experience in biotechnology, pharmaceuticals, medical device organizations.

Parexel

Skills & Focus: Clinical Trials, Biostatistics, Data Management, Statistical Programming, Functional Service Provider, CRA, Epidemiology, Clinical Research Associate, Oncology, Medical Writing
About the Company: Parexel is a global leader in the biopharmaceutical services sector, providing expertise in clinical development and regulatory consulting to improve the quali…
Type: Full-time

Iqvia

Skills & Focus: monitoring, site management, clinical research, Good Clinical Practice, regulatory requirements, study protocol, data quality, recruitment, enrollment, documentation
About the Company: IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industrie…
Experience: 3-5 years of independent on-site monitoring experience.
Type: Full time
Benefits: Benefits programs are designed to meet your total well-being needs so you can thrive at work and at home.

Orchard Therapeutics

Skills & Focus: data analysis, statistical modeling, process analytics, data visualization, GMP data integrity, regulatory compliance, pharmaceutical, gene therapy, data mining, cross-functional teams
About the Company: Orchard Therapeutics is a global gene therapy company dedicated to bringing life-changing therapies to patients with rare diseases.
Experience: Experienced in statistical modeling, multivariate data analysis, and process analytics.
Type: Hybrid

Costello Medical

Skills & Focus: statistical analysis, data analysis, R programming, healthcare, communication skills, project management, client communication, Bayesian methods, clinical trial data, problem solving
About the Company: Costello Medical is a rapidly growing global healthcare agency specialising in medical communications, market access and health economic and outcomes research.…
Experience: An undergraduate degree level or higher qualification in a scientific or mathematical discipline (minimum 2.1 or equivalent) with a focus on statistics and data analysis
Salary: £42,000 per annum
Type: Full-time, permanent
Benefits: Discretionary profit share bonuses paid twice per year, hybrid and flexible working options, generous holiday allowance…

Lindus Health

Skills & Focus: Statistical Strategy Design, Statistical Programming, Clinical Trials, Biostatistics, Management, Leadership, Stakeholder Communication, Statistical Methodologies, Data Management, Healthcare Industry
About the Company: Lindus Health uses software to help innovative companies run faster, more reliable, and patient-friendly clinical trials. Founded in March 2021, the company ha…
Experience: 5+ years of experience in statistics/biostatistics within the clinical or medical research field.
Salary: Competitive salary plus meaningful stock options
Type: Full-time
Benefits: Flexible working, unlimited holidays, £60 monthly wellness allowance, enhanced parental leave, £1,000 Learning and Deve…
Skills & Focus: Statistical Strategy Design, Statistical Programming, Clinical Trials, Biostatistics, Management, Leadership, Stakeholder Communication, Statistical Methodologies, Data Management, Healthcare Industry
About the Company: Lindus Health uses software to help innovative companies run faster, more reliable, and patient-friendly clinical trials. Founded in March 2021, the company ha…
Experience: 5+ years of experience in statistics/biostatistics within the clinical or medical research field.
Salary: Competitive salary plus meaningful stock options
Type: Full-time
Benefits: Flexible working, unlimited holidays, £60 monthly wellness allowance, enhanced parental leave, £1,000 Learning and Deve…

Parexel

Skills & Focus: Biometrics, Global Delivery, Clinical Research, Data Management, Statistical Programmers, Project Leadership, Regulatory Affairs, Clinical Trials, Machine Learning, Research Operations
About the Company: Parexel is a global biopharmaceutical services organization focused on providing innovative solutions to clients in the biopharmaceutical industry.
Type: Full-time

Novartis

Skills & Focus: Risk-based Quality Management, Clinical Trial, Quality Governance, Risk Assessment, Data Management, Audit, Regulatory Requirements, Quality Management Principles, Clinical Protocols, Risk Management Plan
About the Company: Novartis is an innovative medicines company. Every day, we work to reimagine medicine to improve and extend people’s lives so that patients, healthcare profess…

Johnson & Johnson

Skills & Focus: Statistical Programming, programming teams, clinical projects, Biostatistics, data structures, data analytics, project management, clinical development, programming strategy, team leadership
About the Company: At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented,…
Type: Full-time
Skills & Focus: statistical support, analysis, interpretation, design, reporting, data evidence, regulatory, biostatistics, health authority, clinical trials
About the Company: At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented,…
Type: Hybrid
Skills & Focus: Clinical Data Standards, SDTM, Data Management, Regulatory Requirements, Data Transfer, Controlled Terminology, CRF, DTA, CDISC standards, GCP
About the Company: Johnson & Johnson is a multinational corporation focused on healthcare innovation, including pharmaceuticals, medical devices, and consumer health products.
Experience: At least 8 years in pharmaceutical/scientific fields, with minimum 5 years SDTM experience
Type: Full-time