Last updated: 2025-05-01

11 Clinical Operations Management jobs in Barcelona.

Hiring now: Site Activation Coordinat @ Iqvia, Dir Nonclinical And Clini @ Alexion, Global Study Mgr @ Astrazenec, Sr Pharmacovigilance Pv P @ Ergomed, Clinical Study Risk Manag @ Psi, Risk Surveillance Lead @ Novartis.Explore more at jobswithgpt.com. at kaamvaam.com

šŸ”„ Skills

project management (6) collaboration (4) clinical trials (3) compliance (3) clinical development (3) risk management (3) site activation (2) communication (2) regulatory documents (2) clinical research (2)

šŸ“ Locations

Barcelona (11)

Iqvia

Skills & Focus: site activation, clinical trials, healthcare, documentation, compliance, regulatory, project management, communication, interpersonal skills, collaboration
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: Minimum 2 years’ work experience; 1+ years in healthcare or similar
Type: Full-time
Benefits: Benefits programs are designed to meet your total well-being needs so you can thrive at work and at home.

Alexion

Skills & Focus: regulatory documents, NCCP writing, clinical development, medical writers, global regulatory submissions, ICH/GCP guidelines, project management, stakeholder collaboration, mentoring, quality assurance
About the Company: AstraZeneca embraces diversity and equality of opportunity. We are committed to building an inclusive and diverse team representing all backgrounds, with as wi…
Experience: At least 10 years of regulatory MW experience authoring and leading global regulatory submissions.

Astrazeneca

Skills & Focus: Global Study Manager, clinical studies, Haematology, Clinical Study Protocol, study delivery, regulatory compliance, project management, clinical development, vendor management, clinical research
About the Company: AstraZeneca Spain is a rising force in our global business, with headquarters in Madrid and a global hub in Barcelona. It is recognized for its contributions t…
Experience: Minimum of 5 years progressive experience in clinical research, with at least 3 years of clinical development project management experience, or equivalent.
Type: Full time

Alexion

Skills & Focus: Country Study Manager, clinical trials, Good Clinical Practice, regulatory requirements, site activation, monitoring, data deliverables, recruitment targets, clinical development, compliance
About the Company: At AstraZeneca's Alexion division, you will join a team that is dedicated to making a difference in the lives of patients with rare diseases.
Experience: 3+ years of relevant experience gained with a CRO or pharmaceutical company working on clinical studies; Lead CRA/Senior CRA. Management experience preferred.

Astrazeneca

Skills & Focus: Regulatory Affairs, project management, biopharmaceuticals, drug development, submission strategy, multi-disciplinary project teams, regulatory applications, collaboration, innovation, life-changing treatments
About the Company: AstraZeneca Spain is a rising force in our global business, committed to clinical development and the fight against critical disease. It boasts vibrant univers…
Experience: Regulatory experience within the biopharmaceutical industry, or at a health authority, and strong project management skills.
Type: Full time

Alexion

Skills & Focus: regulatory documents, clinical project teams, NCCP, protocols, investigator’s brochures, IND/CTA/NDA submissions, project management, compliance, collaboration, global regulatory requirements
About the Company: To transform the lives of people affected by rare diseases and devastating conditions by continuously innovating and creating meaningful value in all that we d…
Experience: At least 3 years of regulatory MW experience authoring NCCP documents to support global submissions.

Ergomed

Skills & Focus: Pharmacovigilance, ICSR, Signal detection, Risk management, Medical review, Adverse event, Benefit-risk assessment, Regulatory authority, Training, Mentoring

Alexion

Skills & Focus: Good Clinical Practice, clinical trial processes, site monitoring activities, study commitments, regulatory requirements, monitoring oversight, recruitment targets, contract negotiation, project approval, risk management
About the Company: At AstraZeneca's Alexion division, you will join a team that is dedicated to making a difference in the lives of patients with rare diseases. Our innovative sp…
Experience: 3+ years of relevant experience gained with a CRO or pharmaceutical company working on clinical studies; Lead CRA/Senior CRA. Management experience preferred.

Psi

Skills & Focus: risk management, monitoring strategy, centralized monitoring, data integrity, statistical analyses, key risk indicators, study-specific plans, clinical data review, cross-functional environment, data-driven solutions
About the Company: A leading company in clinical monitoring and data integrity.

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.

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…