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

Hiring now: Clinical Research Associa @ Parexel, Srprincipal Clinical Data @ Precision , Proj Spec Clinical Regist @ Iqvia, Srprincipal Clinical Data @ Precision , Sponsor Dedicated Sr Clin @ Syneos Hea, Dir Clinical Strategy Med @ Veeva Syst, Clinical Research Associa @ Lindus Hea, Biostatistics Sr Mgr Hta @ Amgen, Integrated Evidence Team @ Biomarin, Cra Iisr Cra @ Precision .Explore more at jobswithgpt.com.

🔥 Skills

clinical research (10) clinical trials (10) Data Management (7) EDC vendor (6) Clinical Research (5) programming (5) CDISC standards (5) project management (5) Clinical Trials (4) data management (4)

đź“Ť Locations

United Kingdom of Great Britain and Northern Ireland (29)
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Parexel

Clinical Research Associate (CRA) United Kingdom of Great Britain and Nor…
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 Nor…
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 cancer—and we are passionate about helping you harness its power. We strike tumours on a molecular level us…
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.
Senior/Principal Clinical Database Manager United Kingdom of Great Britain and Nor…
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 cancer—and we are passionate about helping you harness its power. We strike tumours on a molecular level us…
Experience: Must have experience in developing and customizing clinical data management databases in a clinical, scientific or health care discipline

Iqvia

Project Specialist - Clinical Registry Coordinator United Kingdom of Great Britain and Nor…
Skills & Focus: clinical registry support, clinical trials, data integration, project management, vendor management, timely delivery, compliance, document submission, disclosure planning, healthcare intelligence
About the Company: IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industri…
Experience: A minimum of 3 years of relevant pharmaceutical/scientific experience in a clinical development environment.
Type: Full time
Benefits: Benefits programs are designed to meet your total well-being needs so you can thrive at work and at home.

Precision Medicine Group

Senior/Principal Clinical Database Manager United Kingdom of Great Britain and Nor…
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 cancer—and we are passionate about helping you harness its power. We strike tumours on a molecular level us…

Parexel

Clinical Program Support Specialist United Kingdom of Great Britain and Nor…
Skills & Focus: clinical trials, project management, global programs, collaboration, budgets, communication skills, oncology studies, clinical research, cross-functional teams, patient well-being
About the Company: Parexel supports clinical studies across the full range of therapeutic areas, and has longstanding partnerships with a vast client base.
Experience: Previous experience supporting global clinical trials; Experience within early phase oncology studies.
Benefits: Supportive work environment, flexible work arrangements, opportunity for career progression.

Syneos Health

Sponsor Dedicated Senior Clinical Editor United Kingdom of Great Britain and Nor…
Skills & Focus: clinical documents, quality control, proofreading, clinical study protocols, data verification, formatting, copyediting, submission standards, style guide, editorial activities
About the Company: Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medic…
Experience: Senior level with SOLID medical/clinical editor experience, QC, and publishing related experience in the pharmaceutical industry.
Benefits: Career development and progression; supportive and engaged line management; technical and therapeutic area training; pe…
Sponsor Dedicated Sr Project Specialist United Kingdom of Great Britain and Nor…
Skills & Focus: Project Management, Clinical Research, Good Clinical Practice, Clinical Trial Operations, Data Management, Regulatory Compliance, Meeting Coordination, Financial Reporting, Customer Engagement, KPI Tracking
About the Company: Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. Our Clinical Development model brin…
Experience: Moderate relevant clinical research experience with an understanding of clinical drug development and clinical trial operations.
Type: Full-time
Benefits: Career development and progression; supportive and engaged line management; technical and therapeutic area training; pe…
Sr Medical Writer United Kingdom of Great Britain and Nor…
Skills & Focus: medical writing, clinical studies, protocols, report writing, regulatory standards, peer review, interpersonal skills, leadership, clinical research, English grammar
About the Company: Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medic…
Experience: Bachelor of Science degree with relevant writing experience or Bachelor of Arts degree (Social Sciences, English or Communications, preferred) with relevant scientific and/or medical knowledge and expertise.
Benefits: Career development and progression; supportive and engaged line management; technical and therapeutic area training; pe…

Precision For Medicine

Regulatory Manager United Kingdom of Great Britain and Nor…
Skills & Focus: regulatory strategy, clinical trials, regulatory submissions, Regulatory Authorities, regulatory guidance, drug development process, regulatory milestones, clinical research, submission targets, ICH GCP
About the Company: Precision for Medicine is a company focused on providing clinical research and consulting services, particularly in regulatory aspects of drug development.
Experience: 5 years Regulatory experience required for the Manager level and 7 years Regulatory experience required for the Senior Manager Regulatory level
Type: Full-time

Iqvia

Global Trial Manager, Late Phase Studies, Single-Sponsor Dedicated United Kingdom of Great Britain and Nor…
Skills & Focus: clinical trials, study management, Vendor Management, project management, patient outcomes, data management, healthcare intelligence, protocol development, regulatory documents, Good Clinical Practice
About the Company: IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industri…
Experience: 2-5 years of experience in managing late phase clinical trials at global level
Type: Full time
Benefits: Benefits programs are designed to meet your total well-being needs so you can thrive at work and at home.

Parexel

Principal Biostatistician United Kingdom of Great Britain and Nor…
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 exc…
Experience: Varies by position (Senior and Principal levels available)
Type: Full-time
Senior Clinical Research Associate United Kingdom of Great Britain and Nor…
Skills & Focus: Clinical Research Associate, Oncology, Site Management, Clinical Trials, Monitoring, GCP/ICH, Interpersonal Skills, Time Management, Problem Solving, Drug Development
About the Company: Parexel supports clinical studies across the full range of therapeutic areas, and we have longstanding partnerships with a vast client base. We supported the t…
Experience: At least 12 months recent oncology experience
Benefits: Flexible work arrangements, career growth and development opportunities

Veeva Systems

Director - Clinical Strategy - MedTech United Kingdom of Great Britain and Nor…
Skills & Focus: clinical data management, clinical operations, MedTech, clinical trials, data management applications, strategic growth, sales support, technology guidance, customer adoption, thought leadership
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 the…
Experience: 5+ years of experience working within the MedTech space through a manufacturer, technology solution provider, or partner.
Type: Full-time
Benefits: Veeva’s support for charitable causes is entirely employee driven, with an annual contribution equivalent to 1% of base…

Precision For Medicine

Senior/Principal Clinical Database Manager United Kingdom of Great Britain and Nor…
Skills & Focus: clinical databases, EDC vendor, Data Management, Project Management, programming, scripting, Microsoft Office, clinical research, data management, leadership
About the Company: Precision medicine is revolutionizing the attack on cancer—and we are passionate about helping you harness its power. We strike tumours on a molecular level us…
Experience: Must have experience in developing and customizing clinical data management databases in a clinical, scientific or health care discipline.

Lindus Health

Clinical Research Associate (CRA) United Kingdom of Great Britain and Nor…
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, £60 monthly wellness allowance, Enhanced Parental Leave, £1,000 Learning and Development allowance,…
Clinical Research Associate (CRA) United Kingdom of Great Britain and Nor…
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, £60 monthly wellness allowance, Enhanced Parental Leave, £1,000 Learning and Development allowance,…

Veeva Systems

Consultant - Clinical Operations United Kingdom of Great Britain and Nor…
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 the…
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 th…

Iqvia

Senior Clinical Research Associate United Kingdom of Great Britain and Nor…
Skills & Focus: clinical research, site monitoring, Good Clinical Practice, International Conference on Harmonization, protocol training, study site practices, regulatory submissions, enrollment, data query resolution, travel flexibility
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: 2-3 years minimum experience of independent on-site monitoring
Type: Full time
Benefits: Benefits programs are designed to meet your total well-being needs so you can thrive at work and at home.

Precision Medicine Group

Senior/Principal Clinical Database Manager United Kingdom of Great Britain and Nor…
Skills & Focus: Clinical Database Manager, Clinical Data Management, EDC vendor, Microsoft Office, Object Oriented Programming, Rave API integration, SAS, CDISC standards, Clinical database management, Leadership skills
About the Company: Precision medicine is revolutionizing the attack on cancer—and we are passionate about helping you harness its power. We strike tumours on a molecular level us…

Amgen

Biostatistics Senior Manager - HTA United Kingdom of Great Britain and Nor…
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.

Precision Medicine Group

Senior/Principal Clinical Database Manager United Kingdom of Great Britain and Nor…
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 cancer—and we are passionate about helping you harness its power. We strike tumours on a molecular level us…
Experience: Must have experience in developing and customizing clinical data management databases in a clinical, scientific or health care discipline.
Senior Clinical Data Manager/Principal Clinical Data Manager United Kingdom of Great Britain and Nor…
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

Iqvia

Clinical Trial Assistant United Kingdom of Great Britain and Nor…
Skills & Focus: Clinical Trial Assistant, clinical research, administrative activities, Trial Master File, Clinical Research Associates, Regulatory and Start-Up, study files, clinical documentation, Case Report Forms, communication
About the Company: IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industri…
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

Integrated Evidence Team Lead, Skeletal Conditions United Kingdom of Great Britain and Nor…
Skills & Focus: integrated evidence plans, cross-functional teams, evidence generation, data interpretation, drug development, market access, health economics, biotech, clinical development, project 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 of related experience in the biotech/pharmaceutical industry, preferably within Rare Disease.
Salary: $205,500 to $308,300 per year
Benefits: A discretionary bonus and/or long-term incentive units may be provided as part of the compensation package, in addition…

Precision Medicine

CRA II/Senior CRA United Kingdom of Great Britain and Nor…
Skills & Focus: CRA, clinical studies, investigative sites, protocol, monitoring, regulatory submissions, site visit, oncology, study risks, quality
About the Company: Precision for Medicine is not your typical CRO. We are passionate about cultivating our culture and are proud to share extremely high CRA retention rates compa…
Experience: At least 2 years CRA experience within the CRO or pharmaceutical industry.

Amgen

Medical Science Liaison - Rare Diseases United Kingdom of Great Britain and Nor…
Skills & Focus: Medical Science Liaison, Rare Diseases, Healthcare Professionals, Scientific Data, Engagement, Clinical Research, Speaker Training, Field Insights, Medical Community, Patient Health Outcomes
About the Company: Amgen is one of the world's leading biotechnology companies focused on researching, manufacturing and delivering innovative products that reach over 10 million…
Experience: Previous Field based experience as MSL or KAM or Sales Rep preferably within rare disease experience.
Type: Full time
Benefits: Generous Total Rewards Plan comprising health, finance and wealth, work/life balance, and career benefits.

Regeneron Pharmaceuticals Inc.

Director, Regulatory Labeling United Kingdom of Great Britain and Nor…
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 bonuses…