Company Description At EVERSANA, we are proud to be certified as a Great Place to Work across the globe. We’re fueled by our vision to create a healthier world. How? Our global team of more than
Axalta has remained at the forefront of the coatings industry by continually investing in innovative solutions. We engineer technologies that protect customers’ products – whether they are battling heat, light, corrosion, abrasion, moisture, or chemicals –
Job Overview: The Aggregate Report Specialist is responsible for supporting core pharmacovigilance deliverables, including scheduled and ad hoc aggregate reports, while ensuring high-quality, timely execution of assigned activities. The role involves collaboration with cross-functional stakeholders, quality
Job Description Reuters is looking for an enthusiastic entry-level Photo Editor with advanced English skills and a sharp eye for detail, capable of sifting through the thousands of images our photographers produce each day. You will
Apprentice Regulatory Certificates, Registration & Religious Barcelona, Spain Do you enjoy being surrounded by regulatory related information and documents? If so, this is the place to be! Here in Regulatory Affairs Documentation Department, we collect all the
Introduction to role: The Local Study Associate Director, Feasibility Lead for Spain and Italy is a key part of the country Cell Therapy Site Management & Monitoring (SMM) organisation. This role supports the feasibility assessment and
“It is critical that we build and maintain our rich tradition of clinical expertise in support of developing life-changing medicines for patients.” –Jose Baselga The Baselga Cancer Research Scholars Program, initiated in 2020, is a 2-year
Role Barcelona onsite - 3 days at the office/2 days at home Company AstraZeneca is a global, innovation-focused biopharmaceutical company dedicated to the discovery, development, and commercialisation of prescription medicines for some of the worlds most
Are you a detail-oriented individual with a passion for research and a good understanding of national and local geography? This freelance opportunity allows you to work at your own pace and from the comfort of your
Join our elite team of Senior Raters as a critical contributor to high-quality validation data that directly influences product development and quality assurance for leading search engines and AI technologies. This flexible, remote opportunity allows you
At Auren Personas we work from the Recruitment & Executive Search division and we are dedicated to providing specialized Human Resources consulting services. Compruebe a continuación si tiene lo necesario para esta oportunidad y, si es
Associate Director, Medical Affairs, Molecular Diagnostics Join to apply for the Associate Director, Medical Affairs, Molecular Diagnostics role at QIAGEN . Overview At QIAGEN, we are driven by a simple but powerful vision: making improvements in life possible.
Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology?At Beckman Coulter Diagnostics, one of Danaher’s 15+ operating companies, our work saves lives—and we’re all united by a
Job OverviewIndividual contributor with advanced knowledge acquired from at least 8 years of relevant industry experience. Recuerde revisar su CV antes de enviar la solicitud. Además, asegúrese de leer todos los requisitos relacionados con este puesto.
Job Title: Executive Director, Regulatory Affairs Strategy - Cell Therapy Available locations: Barcelona, SpainAmsterdam, NetherlandsIntroduction to role: Are you ready to set the global regulatory direction for first-in-class cell therapies and turn science into approved medicines? Do
Executive Director, Regulatory Affairs Strategy - Cell and Gene Therapy Job Title: Executive Director, Regulatory Affairs Strategy - Cell and Gene Therapy Available locations: Barcelona, Spain Amsterdam, Netherlands Introduction to role: Are you ready to set the global
Regulatory Affairs Specialist, Southern Europe Location: Madrid, Spain OR Zaventem, Belgium Hologic is a leading developer, manufacturer, and supplier of diagnostic products, medical imaging systems, and surgical products, with a strong emphasis on serving the healthcare needs
Job Overview Individual contributor with advanced knowledge acquired from at least 8 years of relevant industry experience. Working independently with limited supervision, the individual will provide strategic regulatory expertise and leadership for clinical trial applications and
Rhythm is a global, commercial-stage biopharmaceutical company committed to transforming the lives of patients and their families living with rare neuroendocrine diseases. We develop medicines for previously untreatable or undertreated diseases and provide meaningful support for
Overview As Director, you will shape global regulatory strategy for cell and gene therapies, driving timely approvals and competitive labeling across oncology, immune-mediated and rare diseases. You’ll partner with senior leaders and cross-functional teams to steer