Last updated: 2025-05-22

27 Clinical Operations Management jobs in London.

Hiring now: Mgr Clinical Site Contrac @ Abbvie, Sr Dir Patient Safety Ris @ Astrazenec, Primary Research Coordina @ Clearview , Clinical Ops Leader @ Eucalyptus, Supplier Governance Mgr @ Amgen, Sr Site Contracts Lead Sp @ Syneos Hea, Associate Dir Clinical Me @ Biomarin P, Csr Appendices Oversight @ Novartis, Medical Dir Clinical Deve @ Orchard Th, Recruitment And Screening @ Parexel.Explore more at at kaamvaam.com

šŸ”„ Skills

project management (9) clinical trials (6) clinical research (5) collaboration (5) process improvement (4) negotiation (3) regulatory compliance (3) compliance (3) communication skills (3) reporting (3)

šŸ“ Locations

London (17) High Wycombe (4) Maidenhead (2) Guildford (2) Luton (1) Farnborough (1)

Abbvie

Skills & Focus: clinical contracting, clinical studies, negotiation, regulatory compliance, cross-functional collaboration, contract management, pharmaceutical industry, clinical research, team leadership, process improvement
About the Company: AbbVie is a global biopharmaceutical company focused on discovering and delivering innovative medicines.
Experience: At least 6 years in clinical research or contracting within the pharmaceutical industry
Type: Full-time
Skills & Focus: contract management, clinical study agreements, negotiation, regulatory compliance, budget management, clinical research, contracts, legal review, process improvement, collaboration
About the Company: AbbVie is a global biopharmaceutical company committed to innovative research and development in the healthcare sector.
Experience: At least 5 years in Clinical Research and/or contract/budget experience
Type: Full-time

Astrazeneca

Skills & Focus: patient safety, risk management, regulatory strategies, oncology, collaboration, innovation, health authority, training, methodologies, pharmacovigilance
About the Company: AstraZeneca is one of the world’s most forward-thinking and connected BioPharmaceutical companies, dedicated to delivering life-changing medicines.
Experience: Extensive experience in patient safety/pharmacovigilance and risk management, including applicable industry experience.
Salary: Competitive + Excellent Flexible Benefits!
Type: Full-time
Benefits: Excellent Flexible Benefits

Clearview Healthcare Partners

Skills & Focus: market research, healthcare, biological sciences, expert network, project management, scheduling, communication, consulting, expertise, compliance
About the Company: ClearView Healthcare Partners is a premier life sciences strategy consulting firm headquartered in Boston, with offices in San Francisco, New York City, London…
Experience: Minimum of 1-2 years' work experience in a healthcare-related field or life sciences firm.
Salary: $70,000
Type: Full-time
Benefits: Annual discretionary performance bonus and a comprehensive benefits package.

Eucalyptus

Skills & Focus: clinical operations, weight management, healthcare, prescribing protocols, patient care, performance management, clinical governance, data-driven, digital health, preventive care
About the Company: Eucalyptus is the company behind Juniper, a major weight management program that combines GLP-1 medication with tailored nutrition and exercise, supported by a…
Experience: 7+ years in clinical and commercial environments
Type: Full-time
Benefits: Employee options programme, monthly wellness allowance, personal development budget, enhanced parental leave policy, an…

Amgen

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.

Syneos Health

Skills & Focus: clinical, contract, negotiation, study, budget, patient, site, team, compliance, risk
About the Company: Syneos HealthĀ® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success, translating clinical, medical, and …

Biomarin Pharmaceutical Inc.

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

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

Orchard Therapeutics

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.

Parexel

Skills & Focus: Recruitment, Screening, Clinical Research, Database Management, Communication, Patient Enrollment, Regulatory Compliance, Administrative Support, Volunteer Recruitment, Good Clinical Practice

Costello Medical

Skills & Focus: scientific, project management, medical communications, coordination, scientific documents, client communication, logistics, project support, compliance, collaboration
About the Company: Costello Medical is a rapidly growing global healthcare agency specialising in medical communications, market access, and health economic and outcomes research…
Experience: Minimum 2.1 or equivalent in a scientific discipline; postgraduate qualifications advantageous
Salary: £35,000 per annum
Type: Full-time, permanent
Benefits: Discretionary profit share bonuses, hybrid and flexible working options, generous holiday allowance, private medical in…

Orchard Therapeutics

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.

Pulse Healthcare

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: £40 - £60 per hour
Type: Flexible hours
Benefits: Competitive hourly rates, Daily and weekly payroll services, Revalidation and appraisal services, Access to CPD events …

Orchard Therapeutics

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

Iqvia

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.

Parexel

Skills & Focus: project management, clinical research, regulatory compliance, medical treatments, risk prevention, project plans, GCP, SOPs, medical possibilities, clinical trials
About the Company: Parexel is a global biopharmaceutical services organization dedicated to advancing innovations in medical treatments and therapies.

Novartis

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

Johnson & Johnson

Skills & Focus: statistical support, analysis, interpretation, design, reporting, data evidence, regulatory, biostatistics, health authority, clinical trials
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,…
Type: Hybrid
Skills & Focus: Trial Delivery Management, Oncology, Clinical Trial, Vendor Oversight, Risk Reviews, Phase I-IV, Team Leadership, Project Management, Regulatory, Healthcare
About the Company: A global leader in healthcare and pharmaceuticals, committed to building a world where health is everything.
Skills & Focus: Clinical Project Management, Healthcare, Pharmaceutical, Clinical Trials, Project Management, Budget Management, Team Collaboration, Resource Allocation, Clinical Research, Regulatory Compliance
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: Minimum of 4 years of experience in Pharmaceutical, Healthcare or related industries.
Type: Full-time

Ergomed

Skills & Focus: Global trials, Radiopharmaceuticals, Cancer, Duchenne Muscular Dystrophy, Project delivery, Budget management, Team collaboration, Study planning, Stakeholder liaison, Regulatory standards
Type: Contract
Skills & Focus: clinical, project management, global trials, Radiopharmaceuticals, Cancer, Duchenne Muscular Dystrophy, ALS, Stargardt’s, study activities, regulatory standards
Type: Contract

Syneos Health

Proposal Writer Farnborough
Skills & Focus: proposal writing, business development, clinical trial, technical writing, communication skills, research, project management, customer service, regulatory guidelines, market analysis
About the Company: Syneos HealthĀ® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medic…
Experience: Experience in the CRO, pharmaceutical, or biotechnology industry including technical writing, communications, or marketing experience. Proposal and contract experience strongly preferred.
Type: Full-time
Benefits: Career development and progression; supportive and engaged line management; technical and therapeutic area training; pe…