33 Biopharmaceutical Leadership jobs in Madrid.

Madrid

• Skills: biopharmaceutical, drug development, therapies, Endocrinology, Rare Disease, Oncology, GCP, GVP, Medical Affairs, Regulatory Affairs

Madrid

• Skills: Data Management, Clinical Programming, Remote, FSP, Biomedical Research, Clinical Trials, Data Acquisition, Statistical Programming, Global Inclusion, Biometrics

Madrid

• 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

Madrid

• Skills: Market Access, Price & Reimbursement, HEOR, Oncology, Health Economics, Stakeholder Engagement, Value Proposition, Pricing Strategy, Negotiation Skills, Cross-functional Team
• Experience: Experience in Market Access/Price & Reimbursement/HEOR experience; Previous experience in Oncology filed would be preferred.

Madrid

• Skills: Statistical Programming, SAS, Biostatistics, programmer, leadership, clinical research, data analysis, project management, resource allocation, team management
• Experience: Master's Degree with 5 years relevant experience or Bachelor's Degree with 6 years relevant experience.
• Type: Full time

Madrid

• Skills: pharmacovigilance, EU/UK QPPV, regulatory documents, consultancy services, audits, PV processes, PV training, drug safety, client-facing reports, legislation

Madrid

• Skills: clinical research, project management, pharmaceutical industry, clinical trials, innovation, relationship management, strategic partnerships, oncology, international collaboration, telemonitoring
• Experience: Proven experience in the pharmaceutical industry (working for a pharma or a consulting firm). Experience managing international clinical trials.
• Type: Full time

Madrid

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

Madrid

• Skills: Regulatory Affairs, CMC, Pharmaceutical, Biologics, Quality Control, Submission Strategies, Market Expansions, Risk Management, Collaboration, Technical Documentation
• Experience: Previous experience in regulatory affairs, particularly related to technical/CMC/quality, within the pharmaceutical industry.
• Type: Remote

Madrid

• Skills: medical enquiries, adverse events, document reporting, product quality complaints, medical information database, project status updates, pharmaceutical clients, healthcare professionals, regulatory inspection, pharmacovigilance

Madrid

• Skills: medical monitoring, clinical studies, patient safety, clinical data, SAE reports, medical review, clinical documents, risk assessment, training, collaboration

Madrid

• Skills: Gene Therapy, Medical Affairs, Rare Diseases, Neuro Metabolic Diseases, Scientific Support, Stakeholder Engagement, Clinical Trials, Medical Education, Regulatory Compliance, Biotechnology
• Experience: 3-5 years of Medical Affairs experience with external facing stakeholder engagement within the biotechnology or pharmaceutical industry

Madrid

• Skills: Regulatory Affairs, project management, clinical trials, client relationships, compliance, project execution, budget management, resource planning, cross-functional teams, therapeutic areas
• Experience: extensive experience in Regulatory Affairs, PMP or equivalent certification preferred

Madrid

• Skills: Quality Standards, External Service Providers, Clinical Trials, Quality Assurance, Risk Assessments, Technology Evaluation, Regulatory Compliance, Digital Health, Third-Party Management, Collaboration

Madrid

• Skills: global trials, Radiopharmaceuticals, Gastrointestinal, Lung, Breast Cancer, Duchenne Muscular Dystrophy, ALS, Stargardt’s
• Type: Contract

Madrid

• Skills: medicina innovadora, asesoramiento científico, medicamentos, promoción salud, congresos, PRL, reacción adversa, compliance, CRM, gestión de cartera
• Experience: No prior experience required
• Type: Field-based

Madrid

• Skills: clinical research, GCP, real-world evidence, protocol design, clinical studies, medical monitoring, regulatory submissions, publications, cross-functional collaboration, data management
• Experience: 4+ years of experience in clinical research, including study design and management
• Type: Full time

Madrid

• Skills: regulatory, PV, pharmacovigilance, strategy, project management, compliance, training, regulatory intelligence, inspections, client

Madrid

• Skills: translational research, clinical analytics, digital biomarkers, real-world evidence, AI, healthcare, clinical trials, regulatory compliance, biomarker discovery, cross-functional collaboration
• Experience: 5+ years in translational research, clinical analytics, or digital biomarker development
• Type: Full time

Madrid

• Skills: adverse reactions, medicinal product safety, CAs communication, benefit-risk evaluation, safety studies, marketing authorisations, oversight, safety concerns, Company procedures, post-authorisation

Madrid

• Skills: data strategy, data governance, risk management, compliance, life sciences, pharma industry, stakeholder management, data privacy regulations, clinical trials regulation, AI regulations
• Type: full_time
• Salary: {'min': None, 'max': None, 'period': '', 'currency': ''}

Madrid

• Skills: clinical trials, management, resource allocation, compliance, issue resolution, clinical research, operational management, regulatory requirements, talent development, drug development
• Type: full_time
• Salary: {'min': None, 'max': None, 'period': '', 'currency': ''}

Madrid

• Skills: Pharmacovigilance, Adverse reactions, Regulatory Affairs, Safety processing, Quality Assurance, Safety surveillance, Compliance activities, Medicinal product safety profiles, Communication skills, Project management
• Salary: {'min': None, 'max': None, 'period': '', 'currency': ''}