Last updated: 2025-05-22

22 Clinical Data And Biostatistics jobs in Remote - United Kingdom of Great Britain and Northern Ireland.

Hiring now: Biostatistics Sr Mgr Hta @ Amgen, Srprincipal Clinical Data @ Precision , Clinical Research Associa @ Parexel, Srprincipal Clinical Data @ Precision , Dmsdtm Programmer @ Iqvia, Clinical Research Associa @ Lindus Hea, Consultant Clinical Ops @ Veeva Syst, Sr Clinical Data Mgrprinc @ Pfm, Sr Feasibility Associatef @ Precisionm, Dir Regulatory Labeling @ Regeneron .Explore more at at kaamvaam.com

šŸ”„ Skills

Data Management (7) clinical research (6) programming (6) CDISC standards (6) EDC vendor (5) Clinical Trials (5) scripting (4) data management (4) clinical trials (4) Project Management (3)

šŸ“ Locations

United Kingdom of Great Britain and Northern Ireland (22)
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Amgen

Biostatistics Senior Manager - HTA United Kingdom of Great Britain and Norā€¦
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 deliverā€¦
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.

Precision Medicine Group

Senior/Principal Clinical Database Manager United Kingdom of Great Britain and Norā€¦
Skills & Focus: clinical databases, EDC vendor, Data Management, Project Management, scripting, Object Oriented Programming, clinical research, programming, CDISC standards, database management
About the Company: Precision medicine is revolutionizing the attack on cancerā€”and we are passionate about helping you harness its power. We strike tumours on a molecular level usā€¦
Experience: Must have experience in developing and customizing clinical data management databases in a clinical, scientific or health care discipline.

Parexel

Clinical Research Associate (CRA) United Kingdom of Great Britain and Norā€¦
Skills & Focus: Clinical Research, Oncology, Biostatistics, Data Management, Clinical Trials, Regulatory, FSP, Remote Work, Project Leadership, Global Monitoring
About the Company: Parexel is a global biopharmaceutical services company that provides comprehensive drug development and regulatory consulting services.
Type: Full-time
Benefits: Flexible work arrangement for work-life balance

Precision For Medicine

Senior/Principal Clinical Database Manager United Kingdom of Great Britain and Norā€¦
Skills & Focus: clinical database management, clinical research, data management, EDC vendor, programming, scripting, CDISC standards, object-oriented programming, clinical research tasks, biomarkers
About the Company: Precision medicine is revolutionizing the attack on cancerā€”and we are passionate about helping you harness its power. We strike tumours on a molecular level usā€¦
Experience: Experience in developing and customizing clinical data management databases in a clinical, scientific or health care discipline; Medidata Rave EDC Certified Study Builder; Rave API integration experience.

Iqvia

DM/SDTM Programmer United Kingdom of Great Britain and Norā€¦
Skills & Focus: DM, SDTM, Programmer, clinical trials, data management, SAS programming, data transfer specifications, eCRFs, quality checks, clinical data
About the Company: IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industrieā€¦
Type: Full time

Precision Medicine Group

Senior Clinical Data Manager/Principal Clinical Data Manager United Kingdom of Great Britain and Norā€¦
Skills & Focus: Data Management, Clinical Trials, Database Development, Quality Control, Data Entry, Clinical Research, Project Management, Medical Coding, EDC, SOPs
Experience: Must have worked as a Lead Data Manager for a Clinical Research Organisation or Pharmaceutical company

Precision For Medicine

Senior/Principal Clinical Database Manager United Kingdom of Great Britain and Norā€¦
Skills & Focus: Clinical Database Manager, clinical data management, EDC vendor, Medidata Rave, Rave API, programming, scripting, CDISC standards, drug development, clinical research
About the Company: Precision medicine is revolutionizing the attack on cancerā€”and we are passionate about helping you harness its power. We strike tumours on a molecular level usā€¦
Experience: Must have experience in developing and customizing clinical data management databases in a clinical, scientific or health care discipline
Senior/Principal Clinical Database Manager United Kingdom of Great Britain and Norā€¦
Skills & Focus: clinical database management, clinical data management, EDC, data management, clinical research, programming, scripting, CDISC standards, drug development, object-oriented programming
About the Company: Precision medicine is revolutionizing the attack on cancerā€”and we are passionate about helping you harness its power. We strike tumours on a molecular level usā€¦
Experience: Must have experience in developing and customizing clinical data management databases in a clinical, scientific or health care discipline.
CRA II/Senior CRA United Kingdom of Great Britain and Norā€¦
Skills & Focus: clinical, monitoring, study, protocol, SOPs, ICH-GCP, regulations, oncology, TRAVEL, CRA
About the Company: Precision for Medicine is passionate about cultivating a culture that retains high CRA retention rates and offers a work/life balance, with a focus on precisioā€¦
Experience: At least 2 years CRA experience within the CRO or pharmaceutical industry
Type: Full-time

Precision Medicine Group

Senior/Principal Clinical Database Manager United Kingdom of Great Britain and Norā€¦
Skills & Focus: clinical databases, Data Management, EDC vendor, operational training, programming, clinical research, Object Oriented Programming, scripting language, CDISC standards, database management systems
About the Company: Precision medicine is revolutionizing the attack on cancerā€”and we are passionate about helping you harness its power. We strike tumours on a molecular level usā€¦

Parexel

Senior Clinical Vendor Manager - FSP United Kingdom of Great Britain and Norā€¦
Skills & Focus: Procurement, Clinical, Vendor Management, FSP, Remote, Biostatisticians, Statistical Programmers, Clinical Trials, Regulatory Consultants, Data Managers
Principal Biostatistician United Kingdom of Great Britain and Norā€¦
Skills & Focus: Biostatistics, Clinical Research, Data Management, Regulatory Affairs, Statistical Programming, Project Leadership, Healthcare, Pharmaceutical, Clinical Trials, FSP
About the Company: Parexel is a global clinical research organization that specializes in biostatistics and clinical trials, with a commitment to patient welfare and clinical excā€¦
Experience: Varies by position (Senior and Principal levels available)
Type: Full-time
Clinical Operations Leader United Kingdom of Great Britain and Norā€¦
Skills & Focus: Clinical Trials, Clinical Operations, Functional Service Provider, Oncology, Project Leader, Biostatistics, Statistical Programming, Data Management, Regulatory Consultants, Military Talent Community

Precision Medicine Group

Senior/Principal Clinical Database Manager United Kingdom of Great Britain and Norā€¦
Skills & Focus: Clinical Database Management, EDC vendor, Data Management, Project Management, Medidata Rave, API integration, Object Oriented Programming, CDISC standards, SAS, R
About the Company: Precision medicine is revolutionizing the attack on cancerā€”and we are passionate about helping you harness its power. We strike tumours on a molecular level usā€¦

Lindus Health

Clinical Research Associate (CRA) United Kingdom of Great Britain and Norā€¦
Skills & Focus: clinical trials, monitoring, risk-proportionate, NHS, regulations, stakeholders, site visits, central monitoring, startup environment, patient-friendly
About the Company: We use software to help innovative companies run faster, more reliable, and patient-friendly clinical trials.
Experience: 3+ years in clinical trial monitoring
Salary: Competitive salary, plus meaningful stock options
Type: Full-time
Benefits: Unlimited holidays, Ā£60 monthly wellness allowance, Enhanced Parental Leave, Ā£1,000 Learning and Development allowance,ā€¦

Veeva Systems

Consultant - Clinical Operations United Kingdom of Great Britain and Norā€¦
Skills & Focus: clinical trials, compliance, implementation, eTMF, CTMS, training, solution design, validation, customer success, life sciences
About the Company: Veeva Systems is a mission-driven organization and pioneer in industry cloud, helping life sciences companies bring therapies to patients faster. As one of theā€¦
Experience: Experience working in clinical trials and/or experience working on implementation projects as a consultant for at least one clinical technology solution.
Type: Full-time
Benefits: Stock bonus %, Health & wellness programs, Life Assurance, Veeva charitable giving program, Free lunch on Tuesday in thā€¦

Pfm

Senior Clinical Data Manager/Principal Clinical Data Manager United Kingdom of Great Britain and Norā€¦
Skills & Focus: clinical trial, data management, CRF specifications, database build, quality control, medical coding, SOPs, EDC, database management, regulatory

Precisionmedicinegroup

Senior Feasibility Associate/Feasibility Manager United Kingdom of Great Britain and Norā€¦
Skills & Focus: feasibility analysis, site identification, clinical protocols, study assumptions, client information, feasibility site outreach, post-award feasibility, patient advocacy groups, enrollment modeling, clinical trial
Experience: 5 years

Iqvia

Sr. CRA 1 United Kingdom of Great Britain and Norā€¦
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 industrieā€¦
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.

Pfm

Senior Feasibility Associate/Feasibility Manager United Kingdom of Great Britain and Norā€¦
Skills & Focus: feasibility analysis, site identification, clinical protocols, study assumptions, epidemiology analysis, study delivery, study feasibility, site outreach, post-award feasibility, data analysis
Experience: At least 5 years

Regeneron Pharmaceuticals Inc.

Director, Regulatory Labeling United Kingdom of Great Britain and Norā€¦
Skills & Focus: Regulatory labeling process, Labeling Working Group, labeling strategies, FDA regulations, EMA regulations, labeling documents, clinical trials, risk management, Biotech industry, mentoring
Experience: 10+ years of related Biotech or Pharma industry experience, 6 or more of which are working with labeling is preferred.
Salary: $202,000.00 - $336,600.00
Type: Contract
Benefits: comprehensive benefits which often include health and wellness programs, fitness centers, equity awards, annual bonusesā€¦

Syneos Health

Sr. R Programmer (TEAL Module Development - R/RShiny) United Kingdom of Great Britain and Norā€¦
Skills & Focus: SAS, programming, clinical trial, data listings, validation programming, quality control, documentation, statistical analysis, project management, mentoring
About the Company: Syneos HealthĀ® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medicā€¦
Experience: Extensive programming experience in SAS or other required software, preferably in a clinical trial environment.
Benefits: Career development and progression; supportive and engaged line management; technical and therapeutic area training; peā€¦