27 Clinical Operations Management jobs in London.

London

• 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

London

• Skills: CSR appendices, regulatory submissions, clinical documents, vendor oversight, submission readiness, cross-functional collaboration, audit support, process improvement, clinical document management, timely submissions
• Experience: Relevant industry experience
• Type: Hybrid

London

• 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

London

• Skills: Risk-based Quality Management, Clinical Trial, Quality Governance, Risk Assessment, Data Management, Audit, Regulatory Requirements, Quality Management Principles, Clinical Protocols, Risk Management Plan

High Wycombe

• Skills: statistical support, analysis, interpretation, design, reporting, data evidence, regulatory, biostatistics, health authority, clinical trials
• Type: Hybrid

London

• Skills: Clinical Development, Regulatory Interaction, Gene Therapy, Collaboration, Clinical Strategy, Matrix Team, Regulatory Documents, Clinical Trials, Medical Monitoring, Cross-Functional Team
• Experience: Significant prior experience of working in biotech/pharma or regulatory agency essential.

London

• Skills: vendor, clinical trial, collaboration, study start-up, risk management, protocol development, budget, performance standards, operational procedures, study outcomes
• Type: Hybrid

London

• Skills: regulatory activities, EMA, EU/UK, submissions, clinical trials, biologics, ATMPs, regulatory submissions, drug development, collaboration
• Experience: Minimum of 7 years of regulatory experience, focused on the development of biologics and/or Advanced Therapy Medicinal Products (ATMPs) in the EU/UK.

London

• Skills: Clinical Medical Writing, Medical Writing staff, regulatory submission, clinical development, resource forecasting, vendor management, clinical study reports, protocol design, documentation projects, cross-functional groups
• Experience: At least 10 years of experience as a medical writer in the pharmaceutical industry.
• Type: Full-time

London

• Skills: Acute Medicine, Registrar, GMC registration, NHS experience, Patient care, Clinical protocols, Teaching, Supervision, Clinical audits, Research projects
• Experience: 6 months NHS experience, GMC registration, MRCP, Specialist training started
• Type: Flexible hours
• Salary: £40 - £60 per hour

London

• Skills: market research, healthcare, biological sciences, expert network, project management, scheduling, communication, consulting, expertise, compliance
• Experience: Minimum of 1-2 years' work experience in a healthcare-related field or life sciences firm.
• Type: Full-time
• Salary: $70,000

London

• Skills: data management, clinical trials, product development, design, validation, data quality, trial delivery, collaboration, clinical operations, user acceptance testing
• Experience: 3+ years
• Type: Full-time
• Salary: Competitive salary, plus meaningful stock options

London

• Skills: clinical operations, weight management, healthcare, prescribing protocols, patient care, performance management, clinical governance, data-driven, digital health, preventive care
• Experience: 7+ years in clinical and commercial environments
• Type: Full-time

London

• Skills: scientific, project management, medical communications, coordination, scientific documents, client communication, logistics, project support, compliance, collaboration
• Experience: Minimum 2.1 or equivalent in a scientific discipline; postgraduate qualifications advantageous
• Type: Full-time, permanent
• Salary: £35,000 per annum

London

• Skills: project management, clinical research, regulatory compliance, medical treatments, risk prevention, project plans, GCP, SOPs, medical possibilities, clinical trials

Guildford

• Skills: clinical, project management, global trials, Radiopharmaceuticals, Cancer, Duchenne Muscular Dystrophy, ALS, Stargardt’s, study activities, regulatory standards
• Type: Contract

London

• Skills: clinical trial finance, budgeting, forecasting, vendor invoices, financial trackers, accrual reports, contract negotiations, study budgets, financial summaries, ERP systems
• Experience: 5+ years in clinical trial finance or operations
• Type: Contract

Luton

• Skills: clinical studies, administration, trial management, document management, regulatory, budgeting, communication, organization, multi-tasking, team work

Guildford

• Skills: signal detection, pharmacovigilance, regulatory requirements, communication with regulatory authorities, quality control, signal management tools, record keeping, evaluating signals, drafting reports, medical information
• Salary: {'min': None, 'max': None, 'period': '', 'currency': ''}

London

• Skills: Clinical Trials, Financial Management, Project Leadership, Stakeholder Communication, Regulatory Compliance, Budget Tracking, Clinical Research, Study Administration, Time Management, Organizational Skills
• Type: full_time
• Salary: {'min': None, 'max': None, 'period': '', 'currency': ''}

London

• Skills: Clinical Data Management, Biopharmaceutical, Project management, EDC, Vendor Oversight, Data Quality, Clinical Study Meetings, Timelines, Good Clinical Practices, Data Review Plans
• Type: full_time
• Salary: {'min': 64500.0, 'max': 87200.0, 'period': 'annual', 'currency': 'GBP'}

High Wycombe

• Skills: clinical trials, programming languages, data management, clinical data, CDISC, data model specifications, study-specific reports, regulatory standards, quality control, risk compliance
• Type: full_time
• Salary: {'min': None, 'max': None, 'period': '', 'currency': ''}