Last updated: 2025-05-22

25 Biopharmaceutical Leadership jobs in Madrid.

Hiring now: Pharmacovigilance Medical @ Ergomed, Sr Dir Medical Strategy L @ Iqvia, Mgr Medical Affairs @ Orchard Th, Medical Monitor @ Psicro, Mgr Clinical Data Managem @ Boston Sci, Emea Integrated Brand Val @ Johnson Jo, Sr Site Contracts Lead Sp @ Syneos Hea, Medical Information Assoc @ Primevigil, Various Positions In Biop @ Ascendis P, Associate Dir External Se @ Novartis.Explore more at at kaamvaam.com

🔥 Skills

Regulatory Affairs (5) pharmacovigilance (4) clinical trials (4) project management (4) Medical Affairs (3) regulatory compliance (3) Collaboration (3) clinical research (2) patient-centered (2) Rare Diseases (2)

📍 Locations

Madrid (25)

Ergomed

Skills & Focus: pharmacovigilance, medical writing, PSURs, PBRERs, PADERs, ACOs, DSURs, RMPs, quality documentation, aggregate reports

Iqvia

Skills & Focus: Cardiovascular, clinical research, medical strategy, clinical trials, data-driven, patient-centered, evidence-based, business development, regulatory, presentation skills
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…
Experience: 2+ years clinical research relevant 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.

Orchard Therapeutics

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

Psicro

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

Iqvia

Skills & Focus: Regulatory Affairs, Real World Evidence, Client Leadership, Business Development, Project Leadership, Drug Development, Post Authorisation Safety Studies, Regulatory Landscape, Client Engagement, Consulting
About the Company: Creating a healthier world is our purpose. Diverse expertise, innovation, and powerful capabilities is how we help get there.
Type: Full time
Benefits: Benefits programs are designed to meet your total well-being needs so you can thrive at work and at home.

Ergomed

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

Boston Scientific

Skills & Focus: clinical data management, EDC systems, Medidata Rave, standard operating procedures, quality environment, project management, data review, regulatory compliance, staff training, process improvement
About the Company: A leader in medical science for more than 40 years, committed to solving health industry challenges with innovative medical solutions.
Experience: Minimum 5 years with clinical data management experience
Type: Full-time

Johnson & Johnson

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

Syneos Health

Skills & Focus: clinical, contracts, negotiations, sponsor, site, budget, stakeholders, protocols, regulations, development
About the Company: Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. They provide clinical, medical affa…

Primevigilance

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

Johnson & Johnson

Skills & Focus: clinical trial, oncology, vendor oversight, study management, risk review, patient-centered, regulatory compliance, cross-functional coordination, study deliverables, team leadership
About the Company: A healthcare company focusing on innovative medicine and MedTech solutions.
Experience: 8+ years in pharmaceutical/healthcare, oncology experience, clinical trial management
Type: Full-time
Benefits: Flexible working environment, career development, extensive benefits package
Skills & Focus: medicina innovadora, asesoramiento científico, medicamentos, promoción salud, congresos, PRL, reacción adversa, compliance, CRM, gestión de cartera
About the Company: A multinational corporation in the healthcare sector specializing in innovative medicine and medical technology.
Experience: No prior experience required
Type: Field-based

Ascendis Pharma

Skills & Focus: biopharmaceutical, drug development, therapies, Endocrinology, Rare Disease, Oncology, GCP, GVP, Medical Affairs, Regulatory Affairs
About the Company: Ascendis Pharma is a fast-growing global biopharmaceutical company committed to making a meaningful difference in patient’s lives. We have locations in Denmark…

Johnson & Johnson

Skills & Focus: Regulatory Affairs, pharmaceutical, medicines, variations, review, promotional materials, translation, Documentation, medical, laboratory
About the Company: Johnson & Johnson is a multinational corporation known for its healthcare products, including innovative medicines and medical devices.
Experience: Minimum B2 in English, studying in Pharmacy or Health Sciences, available for a year starting June
Type: Internship

Novartis

Skills & Focus: Quality Standards, External Service Providers, Clinical Trials, Quality Assurance, Risk Assessments, Technology Evaluation, Regulatory Compliance, Digital Health, Third-Party Management, Collaboration
About the Company: Novartis is an innovative medicines company dedicated to reimagining medicine to improve and extend people's lives with medicines that reach more than 250 mill…

Parexel

Skills & Focus: Regulatory Affairs, CMC, Pharmaceutical, Biologics, Quality Control, Submission Strategies, Market Expansions, Risk Management, Collaboration, Technical Documentation
About the Company: Parexel is a global biopharmaceutical services company that provides expertise in regulatory affairs, clinical research, and other related fields to help bring…
Experience: Previous experience in regulatory affairs, particularly related to technical/CMC/quality, within the pharmaceutical industry.
Type: Remote
Benefits: Flexible work arrangements, supportive and inclusive environment, opportunities for career growth.

Iqvia

Skills & Focus: Qualitative Research, Clinical Outcome Assessment, COA, Patient Focused Drug Development, Research Methods, Data Analysis, Instrument Development, Business Development, Survey Design, Team Leadership
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: At least 6 years of experience developing COA instruments and delivering qualitative research.
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

Skills & Focus: Patient Safety, Pharmacovigilance, regulatory compliance, leadership, communication, health authority, risk management, quality management, team development, collaboration
About the Company: AstraZeneca is a global, science-led, patient-focused biopharmaceutical company that focuses on the discovery, development and commercialisation of prescriptio…
Experience: 10y Experience in Bio/pharmaceutical industry within the Pharmacovigilance space.
Type: Full-time
Benefits: An inclusive culture that champions diversity and collaboration, and always committed to lifelong learning, growth and …

Novo Nordisk

Skills & Focus: Medical Affairs, Rare Diseases, Leadership, Medical strategy, Team management, KOL engagement, Pharmaceutical industry, Cross-functional, Scientific expertise, Therapeutic Areas
About the Company: A proud life-science company focused on improving patients' lives, committed to groundbreaking scientific research.
Experience: At least 5 years holding a leadership role

Psi

Skills & Focus: medical, clinical trials, safety, data analysis, pharmacovigilance, FDA, EMEA, ICH, GCP, advisory boards
About the Company: Medical Monitors provide medical input to global clinical studies and advise the teams and business partners, while always focusing on patients' safety and wel…

Parexel

Skills & Focus: Regulatory Affairs, project management, clinical trials, client relationships, compliance, project execution, budget management, resource planning, cross-functional teams, therapeutic areas
About the Company: Parexel is a global biopharmaceutical services organization that provides a broad range of expertise to support the development and market access of innovative…
Experience: extensive experience in Regulatory Affairs, PMP or equivalent certification preferred

Ergomed

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

Iqvia

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

Ergomed

Skills & Focus: global trials, Radiopharmaceuticals, Cancer, Duchenne Muscular Dystrophy, project management, clinical trials, study activities, regulatory standards, stakeholder liaison, bid defense
Type: Contract

Astrazeneca Spain

Skills & Focus: Pharmacovigilance, Agreements, Contracts, Negotiation, Compliance, Collaboration, Safety, Regulatory, Project management, Leadership
About the Company: AstraZeneca Spain is a rising force in our global business. With headquarters in Madrid and a global hub in Barcelona, we’ve become an important international …
Experience: at least 5 years relevant experience (pharmaceutical, regulatory, safety and partnership)
Type: Full-time