7180 English-speaking jobs in Barcelona

About the company Biorce is a pioneering Healthtech company dedicated to revolutionizing drug development through the power of AI. We are passionate about accelerating medical advancements and improving patient outcomes.

About the company Biorce is a pioneering Healthtech company dedicated to revolutionizing drug development through the power of AI. We are passionate about accelerating medical advancements and improving patient outcomes.

About the company Biorce is a pioneering Healthtech company dedicated to revolutionizing drug development through the power of AI. We are passionate about accelerating medical advancements and improving patient outcomes.

About the company Biorce is a pioneering Healthtech company dedicated to revolutionizing drug development through the power of AI. We are passionate about accelerating medical advancements and improving patient outcomes.

About the company Biorce is a pioneering Healthtech company dedicated to revolutionizing drug development through the power of AI. We are passionate about accelerating medical advancements and improving patient outcomes.

The Associate Director, Data Products will set the vision and execute a suite of data products for R&D. This role translates business problems into product capabilities, manages product lifecycles, and ensures measurable value delivery. The successful candidate will partner with stakeholders, create roadmaps, and champion user adoption.

The Senior Manager, Nonclinical and Clinical Pharmacology Writing prepares regulatory-compliant documents for clinical development programs. Responsibilities include authoring protocols, study reports, and other submissions. Requires a science background, preferably pharmacology, with experience in regulatory documentation and medical communications.

Leads execution of the Commercial AI strategy, focusing on AI innovation, adoption, upskilling, and business transformation. Manages cross-commercial transformation programs and collaborates with stakeholders to identify and implement scalable solutions. Designs and delivers tailored upskilling programs across commercial functions. Maintains expertise in emerging technologies and contributes to reimagining the workplace.

Leads statistical design and strategy for product development, clinical studies, and regulatory submissions in cardiovascular, renal, and metabolism. Provides global leadership, mentors staff, and represents statistical strategy in internal governance. Requires a Master's or PhD in Statistics or related field with a track record of independent leadership and exemplary technical skills.

The Global Medical Director will develop and implement global medical strategies for hematology, nephrology, and transplant indications. Responsibilities include leading the development of global product disease strategy plans, overseeing medical strategy and budget, and providing medical guidance to country medical teams. The role requires a PhD, PharmD, or MD degree and 1-4+ years of experience in medical affairs.

Leads global patient advocacy strategy and engagement for Alexion Rare Disease Business unit. Responsible for building and enhancing strategic alliances with patient advocacy organizations to drive patient-centric goals. Collaborates with cross-functional teams to advance patient-focused drug development and ensure patient perspectives are integrated into decision-making. Requires 10+ years of progressive industry experience or 7+ years in patient advocacy, including global/international roles. Solid knowledge of the rare disease advocacy community and the biopharma industry is essential.

Associate Director, Patient Safety Scientist will support safety strategy and requirements for assigned projects in the Vaccines & Immune Therapies Therapeutic Area. Responsibilities include aggregating, reviewing, analyzing, and interpreting safety data to support safety decision-making. The role requires experience in at least 3 of the following areas: clinical drug development, post-marketing surveillance, MAA/BLA submissions, periodic safety reports, risk management plans, and governance board interactions.

Leads cross-functional study teams to ensure clinical study progress according to timelines, budget, and quality standards. Manages study level documents, external service providers, and study budgets. Provides guidance to study team members and mentors less experienced colleagues. Requires a university degree in medical or biological sciences or a related field, at least 7 years of clinical trial experience, and at least 3 years of experience in global study leadership.

Designs, delivers, and supports integration solutions and APIs built on MuleSoft Anypoint Platform. Provides technical support and collaborates with teams to translate business requirements into technical solutions. Manages API landscape and catalogue, and leads integration teams to deliver complex projects.

In this role, you will be the connective tissue between global marketing, market access, and technology—translating strategy into data-driven capabilities that help teams make confident, timely decisions.

The Medical Director, Senior Patient Safety Physician provides strategic input to drug development and post-marketing programs. This role collaborates on safety surveillance activities, ensures projects adhere to regulatory requirements, and leads the safety strategy for regulatory communication.

Leads the development and delivery of health economic models for global HTA submissions. Provides expertise in economic modeling, budget impact analysis, and statistical methods. Contributes to HTA submissions, responds to questions, and supports cross-functional teams.

The Global Pricing Implementation Lead will optimize the implementation of price & market access strategies for AstraZeneca's Respiratory & Immunology (R&I) portfolio. The role will support reimbursement decisions at a local, regional, and global level, collaborating with the Pricing Director and GMAP team. Responsibilities include developing pricing and access strategies, managing pricing policy and governance processes, and providing forward-looking analysis on price assumptions. The role requires extensive experience in the pharmaceutical industry, executing price strategies, and understanding pricing, legal, regulatory, and reimbursement issues.

As a Scriptwriter at QforMedia you will collaborate with our Quantum Tech HD team to craft engaging video content that reaches millions of viewers worldwide. If you have a passion for storytelling, a keen eye for detail, and the ability to turn raw footage into compelling stories, we want to hear from you!

Senior Site Reliability Engineer to design, plan, and lead reliability initiatives across services, squads, and stakeholders. Requires experience scaling systems, leading initiatives across multiple teams, and strong communication skills. Technical background in cloud infrastructure, containers, infrastructure as code, observability, CI/CD, and software engineering. Must be comfortable defining SLOs, using error budgets, leading incident response, and improving production readiness.