48 Clinical Operations Management jobs in London.

Hiring now: Clinical Trial Asst @ Iqvia, Clinical Study Admin @ Astrazenec, Head Protocol And Clinica @ Novartis, Associate Dir Clinical Me @ Biomarin P, Medical Dir @ Apothecom, Sr Clinical Data Mgr @ Precision , Proj Mgr Supply Logistics @ Parexel, Sr Proj Mgr Cdms Implemen @ Veeva Syst, Regulatory Affairs Lead @ Orchard Th, Resourcing Mgr @ Not Specif.Explore more at jobswithgpt.com.

🔥 Skills

clinical trials (16) project management (10) clinical research (7) Clinical Trials (7) stakeholders (6) Oncology (6) Data Management (6) risk management (5) collaboration (5) Good Clinical Practice (5)

đź“Ť Locations

London (35) High Wycombe (5) Luton (4) Farnborough (3) Welwyn Garden City (1)
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Iqvia

Clinical Trial Assistant Welwyn Garden City
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.

Astrazeneca

Clinical Study Administrator Luton
Skills & Focus: clinical research, administration, study activities, document management, Compliance, eTMF, Regulatory Authorities, Coordination, Quality Control, Organizational skills
About the Company: AstraZeneca is one of the world’s most forward-thinking and connected BioPharmaceutical companies, committed to making a difference by treating, preventing, an…
Experience: Previous administrative experience preferably in the medical/life science field.
Senior Director Patient Centered Clinical Trial Luton
Skills & Focus: Patient Centered Development, R&D, stakeholders, clinical trials, patient experience data, global project team, patient engagement, process implementation, metrics and dashboard, strategic thinking
About the Company: AstraZeneca is one of the world’s most forward-thinking and connected BioPharmaceutical companies.
Experience: More than 10 years experience in Pharmaceutical Industry
Director, Site Management & Monitoring (12 Months FTC) Luton
Skills & Focus: clinical studies, project management, interpersonal skills, team development, resource allocation, performance management, quality improvement, ICH-GCP, study site management, medical knowledge
About the Company: AstraZeneca is a global, science-led, patient-focused biopharmaceutical company that focuses on the discovery, development and commercialisation of prescriptio…
Experience: Minimum 5 years of experience in Development Operations (CRA / SrCRA / LSAD) or other related fields.
Type: Full-time
Benefits: Competitive salary and benefits package, including a flexible employee benefits fund, pension contributions, Share Save…

Novartis

Head Protocol and Clinical Program Excellence London
Skills & Focus: strategic planning, operational execution, clinical science, clinical development plans, study protocols, scientific rigor, regulatory requirements, market access, cross functional collaboration, metrics review
About the Company: Novartis is an innovative medicines company dedicated to reimagining medicine to improve and extend people’s lives.
Type: Hybrid

Biomarin Pharmaceutical Inc.

Associate Director, Clinical Medical Writing London
Skills & Focus: Clinical Medical Writing, Medical Writing staff, regulatory submission, clinical development, resource forecasting, vendor management, clinical study reports, protocol design, documentation projects, cross-functional groups
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.
Type: Full-time

Novartis

CSR Appendices Oversight Manager London
Skills & Focus: CSR appendices, regulatory submissions, clinical documents, vendor oversight, submission readiness, cross-functional collaboration, audit support, process improvement, clinical document management, timely submissions
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…
Experience: Relevant industry experience
Type: Hybrid

Biomarin Pharmaceutical Inc.

Senior Business Operations Program Site Manager London
Skills & Focus: budget management, contract negotiation, financial analysis, site operations, clinical trials, cost drivers, stakeholder collaboration, budget templates, payment strategy, risk 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…

Apothecom

Medical Director London
Skills & Focus: medical communications, scientific support, therapeutic area, medical documents, clinical trial data, client communication, literature searches, advisory boards, medical manuscripts, multi-tasking
About the Company: ApotheCom is an exciting leader in the field of medical communications, providing high-quality medical communications programs from a diverse background includ…
Benefits: Attractive rewards package, excellent training and development opportunities, supportive and friendly environment.
Medical Director London
Skills & Focus: medical communications, scientific support, therapeutic area, medical documents, clinical trial data, client communication, literature searches, advisory boards, medical manuscripts, multi-tasking
About the Company: ApotheCom is an exciting leader in the field of medical communications, providing high-quality medical communications programs from a diverse background includ…
Benefits: Attractive rewards package, excellent training and development opportunities, supportive and friendly environment.

Novartis

Central Monitor London
Skills & Focus: clinical trials, monitoring, data quality, risk management, data analytics, regulatory compliance, Good Clinical Practice, collaboration, risk identification, improvement
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…

Precision Medicine Group

Senior Clinical Data Manager London
Skills & Focus: Clinical Data Management, Oncology, Orphan Drug, Clinical Trial, Data Management Plan, Database Development, Quality Control, SOPs, Medical Coding, CDISC Standards
About the Company: Precision Medicine Group is an Equal Opportunity Employer focused on innovative solutions for clinical trials, emphasizing the importance of effective data man…
Experience: 8+ years’ experience
Type: Full-time
Senior Clinical Data Manager London
Skills & Focus: Clinical Data Management, Oncology, Database Development, CRF Specifications, Quality Control, Data Management Plan, Regulatory Directives, Clinical Trial Data, EDC Vendors, SAS Programming
Experience: 8+ years’ experience with strong Oncology and/or Orphan Drug therapeutic experience
Type: Full-time

Parexel

Project Manager Supply & Logistics London
Skills & Focus: Project Manager, Supply Chain, Logistics, Clinical Trials, Remote Work, Project Leadership, Regulatory Affairs, Data Management, Clinical Research, Vendor Management

Biomarin Pharmaceutical Inc.

Senior Business Operations Program Site Manager London
Skills & Focus: budget management, contract negotiation, financial activities, site budgeting, clinical trials, stakeholder collaboration, process improvements, biotechnology, budgets, financial risk
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…

Parexel

Various Positions Available London
Skills & Focus: Clinical Trials, CRA, Functional Service Provider, Data Management, Statistical Programming, Project Leadership, Biostatistics, Oncology, Epidemiology, Site Care Partner

Veeva Systems

Senior Project Manager - CDMS Implementation London
Skills & Focus: project management, clinical trials, data management, EDC clinical software, customer success, implementation, clinical data, life sciences, compliance, stakeholder management
About the Company: Veeva Systems is a mission-driven organization and pioneer in industry cloud, helping life sciences companies bring therapies to patients faster.
Experience: 5+ years’ direct experience working with EDC clinical software solutions in clinical data management
Type: Full-time
Benefits: Additional annual leave over Christmas break, Health & wellness programs

Orchard Therapeutics

Regulatory Affairs Lead London
Skills & Focus: regulatory activities, EMA, EU/UK, submissions, clinical trials, biologics, ATMPs, regulatory submissions, drug development, collaboration
About the Company: Orchard Therapeutics is a global gene therapy leader dedicated to transforming the lives of people affected by rare diseases through the development of innovat…
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.
Clinical Trial Administrator London
Skills & Focus: clinical trials, clinical study managers, project administrative support, communication, documentation, timeline management, budget oversight, team environment, organizational skills, MSOffice
About the Company: Orchard Therapeutics is a global biotechnology gene therapy company dedicated to transforming the lives of people affected by rare diseases through the develop…
Experience: 2-years CTA experience

Biomarin Pharmaceutical Inc.

Associate Director, Clinical Medical Writing London
Skills & Focus: Medical Writing, Regulatory Submission, Clinical Development, Document Authoring, Cross-functional Collaboration, Resource Management, Vendor Management, Clinical Study Reports, Protocol Design, Document Review
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.
Type: Full-time

Biomarin

Senior Business Operations Program Site Manager London
Skills & Focus: site-budget, financial management, contracting, budget negotiations, process improvements, clinical contracts, payments, study protocol, budget analysis, sourcing and selection
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…
Type: Hybrid

Amgen

Supplier Governance Manager London
Skills & Focus: supplier governance, clinical research, biotechnology, project management, process improvement, Good Clinical Practices, FDA regulations, international regulatory guidelines, risk management, collaboration
About the Company: At Amgen, our shared mission—to serve patients—drives all that we do. It is key to our becoming one of the world’s leading biotechnology companies. We are glob…
Experience: Clinical research experience in biopharmaceuticals (biotech, pharma, or CRO)
Type: Flex Commuter / Hybrid
Benefits: Generous Total Rewards Plan comprising health, finance and wealth, work/life balance, and career benefits.

Parexel

Clinical Feasibility Leader London
Skills & Focus: Clinical Trials, Feasibility, Clinical Research, FSP, CRA, Project Leader, Biostatistics, Data Management, Regulatory, Statistical Programming
About the Company: Parexel is a global company dedicated to providing insights that will help deliver safe and effective new therapies to market.

Lindus Health

Clinical Operations Manager London
Skills & Focus: clinical trials, project management, Good Clinical Practice, risk mitigation, team management, clinical operations, study start-up, multi-site trials, technology adaptation, regulatory requirements
About the Company: We use software to help innovative companies run faster, more reliable, and patient-friendly clinical trials. Since founding the company in March 2021, we’ve h…
Experience: >6 years managing and coordinating clinical trials
Salary: Competitive salary plus meaningful stock options
Type: Full-time
Benefits: Flexible working, unlimited holidays, wellness allowance, enhanced parental leave, learning and development allowance, …
Clinical Operations Manager London
Skills & Focus: clinical trials, project management, Good Clinical Practice, risk mitigation, team management, clinical operations, study start-up, multi-site trials, technology adaptation, regulatory requirements
About the Company: We use software to help innovative companies run faster, more reliable, and patient-friendly clinical trials. Since founding the company in March 2021, we’ve h…
Experience: >6 years managing and coordinating clinical trials
Salary: Competitive salary plus meaningful stock options
Type: Full-time
Benefits: Flexible working, unlimited holidays, wellness allowance, enhanced parental leave, learning and development allowance, …

Veeva Systems

Senior Consultant London
Skills & Focus: data management, project management, clinical trial, implementation, configuration, project communication, customer advocate, mentor, project scope, customer success
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: Deep data management/project management and clinical trial expertise
Type: Full-time
Benefits: Work from home or in the office, flexibility

Orchard Therapeutics

Medical Director, Clinical Development London
Skills & Focus: Clinical Development, Regulatory Interaction, Gene Therapy, Collaboration, Clinical Strategy, Matrix Team, Regulatory Documents, Clinical Trials, Medical Monitoring, Cross-Functional Team
About the Company: Orchard Therapeutics is a global biotechnology gene therapy company dedicated to transforming the lives of people affected by rare diseases through the develop…
Experience: Significant prior experience of working in biotech/pharma or regulatory agency essential.

Novartis

Monitoring Excellence Head London
Skills & Focus: Monitoring Excellence, clinical trials, central monitoring, field monitoring, performance metrics, stakeholders, quality assurance, compliance, leadership, cross-functional
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…
Type: Hybrid

Orchard Therapeutics

Clinical Scientist London
Skills & Focus: clinical study documents, protocol writing, clinical trial activities, regulatory environment, GCP/ICH compliance, rare disease, gene therapy, clinical research coordination, data analysis, stakeholder communication
About the Company: Orchard Therapeutics is a global biotechnology gene therapy company dedicated to transforming the lives of people affected by rare diseases through the develop…
Experience: Experience in protocol writing, clinical trial activities, and clinical study report writing, ideally gained through roles such as Clinical Researcher, Clinical Research Associate (CRA), Clinical Trial Assistant (CTA), or Clinical Scientist.
Type: Full-time

Boston Scientific

Clinical Scientist, Fellow - EMEA London
Skills & Focus: clinical trial strategies, regulatory submissions, clinical data interpretation, scientific evidence, study design, collaboration, biostatistics, medical device, Good Clinical Practices (GCP), ISO 14155
About the Company: Boston Scientific is a global leader in medical science, committed to solving significant health industry challenges and transforming lives through innovative …
Experience: Minimum 7 years of experience in clinical research within the medical device industry.
Type: Hybrid

Parexel

Various Positions London
Skills & Focus: Clinical Trials, Clinical Research Associate, Biostatistics, Statistical Programming, FSP, Data Management, Remote, Oncology, Project Leadership, Functional Service Provider
About the Company: Parexel helps accelerate the development of a drug, from concept to commercialization.

Pulse Healthcare

Locum Acute Medicine Registrar London
Skills & Focus: 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
Salary: ÂŁ40 - ÂŁ60 per hour
Type: Flexible hours
Benefits: Competitive hourly rates, Daily and weekly payroll services, Revalidation and appraisal services, Access to CPD events …

Iqvia

Sr. CRA 1 London
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.

Johnson & Johnson

Senior Site Manager High Wycombe
Skills & Focus: Senior Site Manager, Oncology, Clinical Trial Monitoring, Good Clinical Practice, Regulations, Project Manager, Clinical Trial Support, Team Player, Problem Solver, Data Management
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,…
Experience: 2-3 years of clinical trial monitoring experience preferred
Type: Full-time
Benefits: Competitive salary and extensive benefits package. Flexible working environment and career development opportunities.
Senior Manager, Partnership Management High Wycombe
Skills & Focus: Partnership Management, Clinical Research, Project Management, Stakeholder Management, Operational Excellence, Issue Resolution, Collaboration, Communication, Contractual Obligations, Performance Management
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,…
Experience: At least 8 years of relevant industry experience including clinical research and alliance/partnership management in the clinical operations environment.
Type: Hybrid
Sr, Manager, Trial Delivery Leader, Oncology High Wycombe
Skills & Focus: clinical trial delivery, operational oversight, cross-functional team, budget management, timelines, quality, risk management, Health Authority inspections, process improvement, employee engagement
About the Company: Johnson & Johnson is a global leader in healthcare innovation committed to building a world where complex diseases are prevented, treated, and cured.
Experience: Minimum of 8 years in Pharmaceutical, Healthcare or related industries.
Type: Hybrid

Iqvia

Clinical Trial Assistant High Wycombe
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.

Syneos Health

Clinical Trial Specialist Apprentice Farnborough
Skills & Focus: Clinical Trials, Apprentice, Biopharmaceutical, Patient Access, Clinical Operations, Data Management, Pharmacovigilance, Regulatory Affairs, Biometrics, Research
About the Company: Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medic…
Experience: Minimum 5 GCSEs grades 9 to 4 (A* to C) including Maths and English language. Have/be predicted to achieve 80 UCAS points, ideally including Biology and one other science.
Type: Apprenticeship
Benefits: Competitive annual salary, private healthcare, pension.
Sr Site Contracts Specialist Farnborough
Skills & Focus: Contracts Management, Clinical Trials, Budget Negotiation, Clinical Development, Site Contracts, Multi-Country Projects, Quality Control, Contract Templates, Project Management, Regulatory Compliance
About the Company: Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. Our Clinical Development model bring…
Experience: Moderate contracts management experience, preferred management experience.
Type: Hybrid
Benefits: Career development and progression; supportive line management; technical and therapeutic area training; peer recogniti…
Sr Site Contracts Lead Farnborough
Skills & Focus: site contracts, clinical study agreements, negotiations, contractual language, investigator grant budgets, escalation, industry trends, risk mitigation, strategic planning, mentorship
About the Company: Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medic…
Experience: Strong experience in a CRO/pharmaceutical industry and related clinical trial expertise (Study Coordinator, CRA, Pharmacy, Nursing, Healthcare Administration) or site start-up experience.