51 Biopharmaceutical Leadership jobs in Remote - United Kingdom of Great Britain and Northern Ireland.

United Kingdom of Great Britain and Nor…

• Skills: Procurement, Clinical, Vendor Management, FSP, Remote, Biostatisticians, Statistical Programmers, Clinical Trials, Regulatory Consultants, Data Managers

United Kingdom of Great Britain and Nor…

• Skills: monitoring, site management, clinical research, Good Clinical Practice, regulatory requirements, study protocol, data quality, recruitment, enrollment, documentation
• Experience: 3-5 years of independent on-site monitoring experience.
• Type: Full time

United Kingdom of Great Britain and Nor…

• Skills: clinical trials, compliance, implementation, eTMF, CTMS, training, solution design, validation, customer success, life sciences
• 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

United Kingdom of Great Britain and Nor…

• Skills: Biostatistics, Clinical Research, Data Management, Regulatory Affairs, Statistical Programming, Project Leadership, Healthcare, Pharmaceutical, Clinical Trials, FSP
• Experience: Varies by position (Senior and Principal levels available)
• Type: Full-time

United Kingdom of Great Britain and Nor…

• Skills: vendor management, clinical operations, project management, risk management, site activations, vendor deliverables, performance issues, vendor onboarding, KPI, communication
• Type: Full-time

United Kingdom of Great Britain and Nor…

• Skills: supplier governance, clinical research, biotechnology, project management, process improvement, Good Clinical Practices, FDA regulations, international regulatory guidelines, risk management, collaboration
• Experience: Clinical research experience in biopharmaceuticals (biotech, pharma, or CRO)
• Type: Flex Commuter / Hybrid

United Kingdom of Great Britain and Nor…

• Skills: clinical database management, Medidata Rave EDC, Rave API integration, scripting, CDISC standards, clinical research, object-oriented programming, database management systems, leadership, communication skills
• Experience: Must have experience in developing and customizing clinical data management databases in a clinical, scientific or health care discipline.

United Kingdom of Great Britain and Nor…

• Skills: Clinical Database Manager, Clinical Data Management, EDC vendor, Microsoft Office, Object Oriented Programming, Rave API integration, SAS, CDISC standards, Clinical database management, Leadership skills

United Kingdom of Great Britain and Nor…

• Skills: clinical databases, EDC vendor, Data Management, Project Management, programming, scripting, Microsoft Office, clinical research, data management, leadership
• Experience: Must have experience in developing and customizing clinical data management databases in a clinical, scientific or health care discipline.

United Kingdom of Great Britain and Nor…

• Skills: Clinical Database Management, EDC vendor, Data Management, Project Management, Medidata Rave, API integration, Object Oriented Programming, CDISC standards, SAS, R

United Kingdom of Great Britain and Nor…

• Skills: medical affairs, rare diseases, medical strategy, collaboration, cross-functional, scientific interactions, real-world evidence, patient access, clinical research, biotech
• Experience: 7-10 years
• Type: Full time

United Kingdom of Great Britain and Nor…

• Skills: clinical trials, monitoring, risk-proportionate, NHS, regulations, stakeholders, site visits, central monitoring, startup environment, patient-friendly
• Experience: 3+ years in clinical trial monitoring
• Type: Full-time
• Salary: Competitive salary, plus meaningful stock options

United Kingdom of Great Britain and Nor…

• Skills: medical writing, medical communications, healthcare, content development, cardiovascular therapy, quality control, scientific accuracy, client-centric, medical education content, diversity and inclusion
• Experience: Prior experience working as a medical writer for a medical communications agency
• Type: Hybrid/Remote

United Kingdom of Great Britain and Nor…

• Skills: 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.
• Type: Contract
• Salary: $202,000.00 - $336,600.00

United Kingdom of Great Britain and Nor…

• Skills: life sciences, research, health economics, public health, evidence strategy, business development, quantitative research, qualitative research, healthcare, patient-centric
• Salary: Competitive + excellent benefits

United Kingdom of Great Britain and Nor…

• Skills: feasibility analysis, site identification, clinical trials, pre-award, post-award, site outreach, feasibility projects, biotech, pharma, biopharmaceutical
• Experience: 5 years

United Kingdom of Great Britain and Nor…

• Skills: 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

United Kingdom of Great Britain and Nor…

• Skills: Compliance, MHRA, IPHA, Signatory, Aesthetic Medicine, Regulations, Governance, Audits, Legal Counsel, Medical
• Experience: 5+ years of Final Signatory experience in UK & Ireland

United Kingdom of Great Britain and Nor…

• Skills: feasibility analysis, clinical protocols, site identification, pre-award, post-award, rescue, site outreach, study analysis, biotech, pharma
• Experience: At least 5 years of related experience

United Kingdom of Great Britain and Nor…

• Skills: Medical Content, Medical Information, SaaS, Cloud solutions, Medical Affairs, P&L, go-to-market strategy, product innovation, thought leadership, customer success
• Type: full_time
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