34 Biopharmaceutical Leadership jobs in Madrid.

Hiring now: Regulatory Affairs Mgr Cm @ Parexel, Sr Mgr Market Access @ Jazz Pharm, Clinical Partnerships Mgr @ Resilience, Regulatory Affairs Dir @ Astrazenec, Lead Trial Delivery Mgr I @ Johnson Jo, Clinical Scientist Fellow @ Boston Sci, Principalsr Regulatory Me @ Syneos Hea, Tactical And Operational @ Iqvia, Various Positions In Biop @ Ascendis P, Associate Regulatory And @ Precision .Explore more at jobswithgpt.com.

🔥 Skills

clinical research (6) clinical trials (6) project management (5) collaboration (5) Regulatory Affairs (4) study design (4) regulatory submissions (4) Medical Affairs (4) CMC (3) Clinical Research (3)

📍 Locations

Madrid (34)

Parexel

Skills & Focus: Regulatory Affairs, CMC, Biologics, Project Leadership, Clinical Research, Data Management, Statistical Programming, Consulting, Medical Writing, Biostatistics
About the Company: Parexel is a global biopharmaceutical services organization that provides a range of services to enhance the clinical development of drugs and medical devices.
Type: Full-time

Jazz Pharmaceuticals

Skills & Focus: Market Access, Price & Reimbursement, HEOR, Oncology, Health Economics, Stakeholder Engagement, Value Proposition, Pricing Strategy, Negotiation Skills, Cross-functional Team
About the Company: Jazz Pharmaceuticals is a global biopharma company whose purpose is to innovate to transform the lives of patients and their families. We are dedicated to deve…
Experience: Experience in Market Access/Price & Reimbursement/HEOR experience; Previous experience in Oncology filed would be preferred.
Benefits: Eligible to participate in various benefits offerings, including medical, dental and vision insurance, retirement savin…

Resilience Care

Skills & Focus: 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

Astrazeneca

Skills & Focus: regulatory affairs, drug development, health authority interactions, global regulatory lead, NDA, strategic leadership, cross-functional teams, clinical strategy, product lifecycle management, collaboration
About the Company: AstraZeneca Spain is a rising force in our global business. With headquarters in Madrid and our global hub in Barcelona, we’ve become an important internationa…
Experience: At least 7-year experience of regulatory drug development or equivalent, and experience with major Health Authority interactions.
Type: Full time
Skills & Focus: HTA, Modelling, Statistical analysis, Data interpretation, Evidence synthesis, Comparative effectiveness, Indirect comparisons, Oncology, Meta-analysis, Health Economics
About the Company: AstraZeneca Spain is a rising force in our global business, with headquarters in Madrid and a global hub in Barcelona. We are committed to clinical development…
Experience: Prior experience working in consultancy or industry in applying expertise to support HTA submissions.
Type: Full time

Johnson & Johnson

Skills & Focus: clinical trials, vendor management, risk reviews, trial management, training, project planning, communication, analytical skills, team leadership, milestone tracking
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 clinical trial experience in Pharmaceutical or Healthcare; Minimum of 2-3 years’ experience supporting multiple aspects of a global clinical trial.
Type: Hybrid

Boston Scientific

Skills & Focus: clinical trial, study design, data interpretation, regulatory submissions, medical devices, clinical research, scientific evidence, cross-functional collaboration, Good Clinical Practices, biostatistics
About the Company: Boston Scientific is a leader in medical science, committed to innovating medical solutions that improve patient lives.
Experience: Minimum 7 years of experience in clinical research within the medical device industry.
Salary: competitive salary based on market insights
Type: Hybrid
Benefits: Opportunities for professional growth, cross-functional collaboration, and meaningful impact in shaping the future of c…

Syneos Health

Skills & Focus: medical writing, clinical study protocols, clinical development plans, regulatory standards, ICH-E3 guidelines, statistical analysis plans, clinical literature searches, peer reviewer, patient narratives, NDA submissions
About the Company: Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success.
Type: Full-time

Astrazeneca

Skills & Focus: clinical program strategy, drug development, project management, collaborators, regulatory agencies, clinical trial data, operational delivery, team collaboration, innovative approaches, biopharmaceutical
About the Company: AstraZeneca Spain is a rising force in our global business with a focus on clinical development and innovation in the biopharmaceutical industry.
Experience: At least 10 years or equivalent experience in drug development leadership.
Type: Full time

Syneos Health

Skills & Focus: medical writer, clinical study protocols, clinical reports, IND submissions, regulatory standards, clinical development, medical writing activities, statistical analysis, peer reviewer, clinical literature searches
About the Company: Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medic…
Experience: Bachelor of Science degree with relevant writing experience or Bachelor of Arts degree (Social Sciences, English or Communications, preferred) with relevant scientific and/or medical knowledge and expertise.
Salary: $60,930.00 to $115,100.00
Type: Full-time
Benefits: Health benefits to include Medical, Dental and Vision, Company match 401k, eligibility to participate in Employee Stock…
CRA II Madrid
Skills & Focus: Clinical Research, Ophthalmology, GCP Compliance, Clinical Trials, Regulatory Documents, Serious Adverse Event, Clinical Study Reports, Monitoring, Data Integrity, Recruitment
About the Company: Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medic…
Experience: 4-6 years of general pharmaceutical industry or clinical research experience, and 2-3 years of monitoring experience.

Astrazeneca

Skills & Focus: Statistical Analysis Plan, preclinical studies, clinical programmes, regulatory submissions, modeling and simulation, statistical methodology, quality improvement, data transformation, team collaboration, pharmaceutical industry
About the Company: AstraZeneca Spain is a rising force in our global business. With headquarters in Madrid and our global hub in Barcelona, we’ve become an important internationa…
Experience: MSc/PhD in Statistics, Mathematics (containing a substantial statistical component), or recognized equivalent to stats MSc. Experience of design, analysis, and reporting of preclinical or clinical studies in more than one setting.
Type: Full time

Syneos Health

Skills & Focus: Clinical Research, Regulatory Documents, Site Selection, Feasibility, Informed Consent, Medical Terminology, Clinical Data, ICH/GCP, Communication Skills, Organizational Skills
About the Company: Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medic…
Experience: 3-4 years
Type: Full-time
Benefits: Career development and progression; supportive and engaged line management; technical and therapeutic area training; pe…

Iqvia

Skills & Focus: clinical trials, project management, study management, clinical research, customer satisfaction, risk management, collaboration, financial success, communication, problem solving
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: 5 years of prior relevant experience including > 1 year project management 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: Regulatory Affairs, CMC, Life Sciences, Biopharmaceuticals, Quality Assurance, Submission Strategies, Technical Documentation, Project Management, Risk Mitigation, Collaboration
About the Company: Parexel is a global biopharmaceutical services organization that provides expertise and solutions to companies in the life sciences sector, helping them to nav…
Experience: Previous experience in regulatory affairs, particularly related to technical/CMC/quality, within the pharmaceutical industry.
Type: Remote
Benefits: Flexible work arrangements, opportunities for career growth, and a supportive work environment.

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…

Boston Scientific

Skills & Focus: clinical trial strategies, study design, scientific data, regulatory requirements, data interpretation, clinical research, medical devices, biostatistics, scientific collaborations, Good Clinical Practices
About the Company: Boston Scientific is a leader in medical science, committed to solving the challenges that matter most in healthcare. With over 40 years of experience, the com…
Experience: Minimum 7 years of experience in clinical research within the medical device industry.
Salary: competitive salary based on market insights
Type: Hybrid
Benefits: Opportunities for professional growth, cross-functional collaboration, and meaningful impact in shaping the future of c…

Parexel

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

Johnson & Johnson

Skills & Focus: clinical trials, Interventional Oncology, medical technology, hospital procedures, teamwork, collaboration, problem-solving, training, clinical operations, KOL development
About the Company: Johnson & Johnson is a healthcare company that emphasizes innovation to create impactful healthcare solutions, mainly focusing on complex diseases.
Experience: Seven or more years of professional experience in the healthcare industry.
Type: Field-based

Iqvia

Skills & Focus: literature requests, adverse event reports, medical and scientific literature, information technology, vendor contract negotiation, training classes, database searches, business news alert, product information support, strategic marketing initiatives
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: 3 years relevant experience or equivalent combination of education, training and 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.

Precision For Medicine

Skills & Focus: regulatory, clinical trial, submission, IRB, ethics committee, informed consent, site activation, budget negotiation, GCP, project management
About the Company: Precision for Medicine is not your typical CRO. At Precision for Medicine we have brought together new technologies, expertise and operational scale to help th…
Experience: Entry level

Johnson & Johnson

Skills & Focus: Medical Affairs, Professional Medical Education, Leading Specialists, scientific communication, Clinical activities, therapeutic area, healthcare innovation, medical education, advisory boards, Market Access
About the Company: Johnson & Johnson is a global healthcare company that believes health is everything. It is dedicated to innovating across the full spectrum of healthcare solut…
Type: Field-based

Iqvia

Skills & Focus: Native Level of Norwegian, updating medicine databases, quality control, documentation, data classification, standardization, collaboration, attention to detail, organizational skills, communication skills
About the Company: Creating a healthier world is our purpose. Diverse expertise, innovation, and powerful capabilities is how we help get there.
Experience: Relevant work experience with databases.
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

Skills & Focus: Medical Education, Healthcare Professionals, Educational Strategy, Therapeutic Areas, Medical Affairs, Networking, Compliance, Digital Formats, Advisory Boards, Educational Grants
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

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.

Boston Scientific

Skills & Focus: clinical trial strategies, study design, scientific data interpretation, regulatory submissions, market approvals, clinical research, Good Clinical Practices, ISO 14155, FDA regulations, evidence-based decision-making
About the Company: Boston Scientific is a global leader in medical science for more than 40 years, committed to solving the challenges that matter most – united by a deep caring …
Experience: Minimum 7 years of experience in clinical research within the medical device industry.
Salary: competitive salary based on the market insights
Type: Hybrid
Benefits: Opportunities for professional growth, cross-functional collaboration, and meaningful impact.

Parexel

Skills & Focus: Regulatory Affairs, CMC, Biologics, Pharmaceuticals, Submission Strategies, Quality Control, Risk Management, Project Management, Technical Documentation, Collaboration
About the Company: Parexel is a global biopharmaceutical services company that helps clients navigate the complex and ever-changing regulatory landscape.
Experience: Previous experience in regulatory affairs, particularly related to technical/CMC/quality, within the pharmaceutical industry.
Type: Remote/Office-based

Precision For Medicine

Skills & Focus: regulatory, site start-up, clinical trial, submission, Informed Consent Form, Essential Document, contract negotiation, audit readiness, clinical operations, project management
About the Company: At Precision for Medicine we have brought together new technologies, expertise and operational scale to help the life sciences improve the speed, cost and succ…
Experience: Entry level
Type: Full-time

Boston Scientific

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

Jazz Pharmaceuticals

Skills & Focus: medical affairs, real-world evidence, RWE studies, evidence generation, cross-functional teams, stakeholder engagement, financial management, compliance, operational excellence, clinical standards
About the Company: Jazz Pharmaceuticals is a global biopharma company whose purpose is to innovate to transform the lives of patients and their families. They are dedicated to de…
Experience: Substantial experience in the pharmaceutical industry in either medical affairs or clinical operations/development
Type: Full-time
Benefits: Medical, dental and vision insurance, retirement savings plan, and flexible paid vacation.

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…

Ergomed

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

Pfizer

Skills & Focus: oncology, hematology, pharmaceutical marketing, strategic planning, portfolio management, customer insights, cross-functional collaboration, budget management, supply chain management, product launch
About the Company: Pfizer is a patient-centric company dedicated to transforming the lives of patients with their diverse portfolio of pharmaceutical products.
Experience: 6+ years of experience in oncology/hematology pharmaceutical marketing
Type: Full time