136 Biopharmaceutical Leadership jobs in London.

London

• Skills: Statistical Strategy Design, Statistical Programming, Clinical Trials, Biostatistics, Management, Leadership, Stakeholder Communication, Statistical Methodologies, Data Management, Healthcare Industry
• Experience: 5+ years of experience in statistics/biostatistics within the clinical or medical research field.
• Type: Full-time
• Salary: Competitive salary plus meaningful stock options

London

• Skills: Medical Writing, Hepatology, Medical Communications, Technical Materials, Client-facing, Scientific Meetings, Life Sciences, Competitive Intelligence, Career Development, Diversity and Inclusion
• Experience: Previous experience working in a Medical Writing role within a medical communications agency environment
• Type: Hybrid or Remote

London

• Skills: Client Management, Project Leadership, Team Management, Financial Oversight, Content Quality, Business Growth, Medical Education, Client Services Role, Pharma Regulations, Strategic Planning
• Experience: Previous experience in a client services role within a medical education / medcomms agency, with well honed project and client management skills.
• Type: Full-time

London

• Skills: health economics, outcomes research, evidence synthesis, systematic literature reviews, economic model development, business development, consulting, team development, client management, methodological expertise
• Experience: 10+ years’ experience in high-impact HEOR publications, business development, consulting, and/or leadership, including a proven track record of success
• Type: Full-time

London

• Skills: CMC strategy, cross-functional team, risk register, product profiles, regulatory submissions, GMP compliance, drug development, stakeholder management, project management, cell & gene therapies
• Experience: Substantial Biotech/Pharmaceutical industry experience including demonstrated experience leading a multidisciplinary CMC team in a matrix setting

London

• Skills: Consulting, R&D, Regulatory Affairs, Clinical Strategy, Operational Delivery, Pharmacovigilance, Workstreams Management, Stakeholder Engagement, Digital Innovation, Life Sciences
• Type: Full-time

London

• Skills: Medical Writing, life sciences, scientific deliverables, publications, training materials, slide sets, interactive content, conference booths, competitive intelligence, KOL communication
• Experience: Previous experience working in a Medical Writing role, within a medical communications agency environment.
• Type: Full-time

Bracknell

• Skills: Ecotoxicology, Endocrine Disruption, Data Analysis, Regulatory Compliance, Technical Leadership, CRO Management, Global Strategy, Research Collaboration, Dataset Interpretation, Innovative Strategies

London

• Skills: clinical trials, data management, CDISC, SDTM, product development, data cleaning, trial delivery, customer support, multi-disciplinary, startup environment
• Experience: 4+ years in data management for clinical trials
• Type: Full-time

London

• Skills: market access, health economics, stakeholder engagement, economic modeling, reimbursement strategies, cross-functional teams, negotiations, health technology assessment, evidence-based medicine, analytical skills
• Experience: 5-7 years of experience in market access, health economics
• Type: Full-time

London

• Skills: health economics, UK HTA processes, project management, health technology assessment, consulting, client engagement, biostatistics, epidemiology, multi-disciplinary professionals, life sciences
• Experience: 10+ years of experience in designing and executing health economic studies and leading clients through UK HTA processes
• Type: Full time

London

• Skills: CMC Regulatory Affairs, project management, healthcare products, medical devices, cosmetics, regulatory strategies, product development, quality management, technical documentation, compliance
• Experience: Minimum of 7 years of relevant work experience, preferably in CMC Regulatory Affairs or R&D.

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: Regulatory Affairs, CMC, biologics, Clinical Research, Data Science, Advanced Analytics, Consulting, Clinical Trials, Project Leadership, Biostatistics

London

• Skills: Regulatory Affairs, Real World Evidence, Client Leadership, Business Development, Project Leadership, Drug Development, Post Authorisation Safety Studies, Regulatory Landscape, Client Engagement, Consulting
• Type: Full time

London

• Skills: ecotoxicology, environmental toxicology, risk assessments, data analysis, technical research, data gathering, project management, regulatory documentation, environmental exposure modeling, IUCLID
• Type: Hybrid

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: clinical writing, medical writing, regulatory submissions, clinical development, document management, cross-functional collaboration, vendor management, team leadership, scientific expertise, budgeting
• Experience: At least 10 years of experience as a medical writer in the pharmaceutical industry. Minimum of 3 years administrative and/or functional management experience.
• Type: Hybrid

High Wycombe

• Skills: Regulatory Affairs, Labeling, Pharmaceutical, Compliance, Project Management, Innovation, Hybrid Work, Scientific Discipline, Patient Labeling, Continuous Improvement
• Experience: A minimum of 8 years of professional work experience is required.
• Type: Hybrid

London

• Skills: Clinical Trials, Biostatistics, Data Management, Statistical Programming, Functional Service Provider, CRA, Epidemiology, Clinical Research Associate, Oncology, Medical Writing
• Type: Full-time

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: strategic initiatives, sourcing strategies, risk mitigation, stakeholder communication, project management, cross-functional collaboration, market analysis, pharmaceutical, business development, team management
• Experience: Managerial experience; experience in account management, sales, sourcing, business development or product management; pharmaceutical or healthcare experience preferable.

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: medical editing, medical communications, scientific literature, regulatory guidelines, editorial processes, accuracy, clarity, therapeutic areas, interpersonal skills, expertise
• Experience: Significant experience as a Medical Editor within a medical communications agency.
• Type: Fixed-term contract

Bracknell

• Skills: mammalian toxicology, toxicology studies, regulatory requirements, technical strategies, stakeholder management, technical leadership, innovative strategies, training development, science-led, product safety

London

• Skills: computational biology, drug discovery, machine learning, advanced analytics, genetic insights, biomarkers, patient stratification, multi-omics, mentorship, cross-functional collaboration
• Experience: 7+ years applying expertise in computational biology
• Type: hybrid
• Salary: $276,500 - $337,500 USD; $351,000 - $429,000 CAD; £220,000 - £268,000 GBP

Guildford

• Skills: pharmacovigilance, regulations, EU/UK QPPV, PV processes, audits, gap analysis, consultancy services, training, drug safety, client-facing reports

London

• Skills: Pharmacovigilance, Safety Assessment, Adverse Event, Data Management, Regulatory Compliance, Vendor Oversight, Process Improvement, Case Processing, Training, Collaboration
• Type: Full-time

London

• Skills: medical writing, scientific content, pharma, biotech, stakeholder engagement, project management, strategic thinking, healthcare communication, regulatory guidelines, content development
• Experience: 3 – 5 years’ experience in medical writing
• Type: Full-time

High Wycombe

• Skills: Regulatory Affairs, Labeling, Pharmaceutical, Documentation, Compliance, Project Management, Scientific Communication, Continuous Improvement, Global Labeling Strategy, Team Leadership
• Experience: 8 years of professional work experience required, with 6 years of direct regulatory labeling content experience.
• Type: Hybrid

London

• Skills: Medical Writing, Clinical Development, Regulatory Submissions, Document Management, Vendor Management, Authoring, Editing, Therapeutics, Clinical Studies, Project Management
• Experience: 10 years of experience as a medical writer in the pharmaceutical industry
• Type: Full-time

London

• Skills: medical affairs, global strategies, stakeholder engagement, collaboration, regulatory compliance, budget management, product launches, lifecycle management, business acumen, cross-functional teams
• Experience: Qualified Medical Doctor (MD) with regional and ideally global portfolio/product medical affairs leadership roles within the pharmaceutical/biotechnology industry.

London

• 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

London

• Skills: Senior Medical Writer, Publications, Scientific expertise, Lung cancer, Technical materials, Client communication, KOL, Scientific meetings, Medical Writing, Medical communications
• Experience: Experience in publications is necessary.

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: Market Access, Health Economics, Reimbursement Strategies, Stakeholder Engagement, Evidence-based Medicine, Economic Modeling, Negotiations, Cross-Functional Teams, Health Technology Assessment, Strategic Thinking
• Experience: A minimum of 5-7 years of experience in market access, health economics, with working knowledge of reimbursement systems in key European countries.
• Type: Full-time

London

• Skills: health economics, outcomes research, evidence synthesis, systematic literature reviews, economic model development, business development, consulting, leadership, methodological input, client management
• Experience: 10+ years
• Type: Full-time

London

• Skills: Supply Planning, GMP, Inventory Management, Demand Planning, Clinical Operations, Manufacturing Planning, Strategic Initiatives, Regulatory Frameworks, Collaboration, Continuous Improvement
• Experience: At least 12 years of end-to-end supply chain experience with a minimum of 5 years in biotechnology or pharmaceuticals.
• Type: Full-time

London

• Skills: Medical Information, Medical Content Development, Scientific Response Documents, Medical Affairs, Medical Communications, Document Management, Collaboration, Medical Writers, Compliance, Client Engagement
• Type: Full-time

London

• Skills: scientific leadership, medical affairs, obesity, hepatology, medical communications, content delivery, strategic documents, client services, advisory boards, team mentoring
• Type: remote, hybrid or in-office

Maidenhead

• Skills: regulatory submissions, medicinal products, cross-functional, compliance, packaging, labeling, EU regulatory procedures, global experience, RIM systems, chance for growth
• Experience: 5+ years of experience in Regulatory Affairs, with a clear focus on medicinal products

London

• Skills: Qualitative Research, Market Research, Pharmaceuticals, Medical Technology, Diagnostics, Project Management, Client Briefing, Discussion Guide, Results Reports, Interdisciplinary Team

High Wycombe

• Skills: commercial strategy, launch readiness, market access, product branding, health economics, stakeholder engagement, budget management, team leadership, regulatory strategy, performance evaluation
• Type: Full-time

London

• Skills: Value Communications, HTA dossiers, market access, medical writing, health technology assessment, client engagement, peer-reviewed manuscripts, leadership, economics evidence, project management
• Experience: 7+ years

London

• Skills: Medical Affairs, Scientific Strategy, Solid Tumour, KOL, Data Generation, Publication Planning, Healthcare compliance, Cross functional collaboration, Training material, Regulatory frameworks

London

• Skills: medical writing, editorial proficiency, scientific understanding, client counsel, project outcomes, high standards in grammar, attention to detail, creative approach, communication excellence, team player
• Experience: Some medical writing experience
• Type: Hybrid

London

• Skills: medical writing, scientific data, client relationships, project management, medical communications, healthcare strategy, content development, review and feedback, mentoring, team management

London

• Skills: Medical Writing, Editorial Proficiency, Scientific Leadership, Client Counsel, Account Management, Project Outcomes, Mentoring, New Business Development, Team Collaboration, Healthcare Communication
• Type: Hybrid

London

• Skills: clinical trials, product management, user research, stakeholder engagement, product strategy, healthcare delivery, regulatory frameworks, empirical analysis, feature definition, cross-functional collaboration
• Experience: 4+ years as a product manager
• Type: Full-time
• Salary: Competitive salary

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: medical communications, pharmaceutical, scientific data, editorial deliverables, client services, project management, mentorship, life sciences, quality control, communications
• Experience: Relevant writing experience in a medical communications/pharmaceutical role
• Type: Full-time

London

• Skills: HTA dossiers, Market Access, health economic evidence, value narratives, disease burden, clinical trial results, patient-reported outcomes, cost-effectiveness, medical writing, global payer environment
• Experience: 7+ years

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: client management, project management, medical communications, client service, team collaboration, budget management, scientific accuracy, medical education, proposal development, healthcare environment
• Experience: Three years’ experience of medical communications or equivalent

London

• Skills: strategic partnerships, life sciences, government, public sector, clinical research, relationship building, cross-Government, stakeholder engagement, public health, vaccine

London

• Skills: medical, communications, healthcare, medical writing, adverse events, product complaints, drug information, medical literature, customer service, call centre
• Type: Full-time