Revolution Medicines is a global, commercial-state oncology company dedicated to discovering, developing and delivering innovative medicines for patients with RAS-addicted cancers. Leveraging its differentiated RAS(ON) tri-complex inhibitor platform, the company is advancing a broad, integrated portfolio
Please submit your application in English What Youll Do: Support of Regulatory Affairs Study Start-Up (RASSU) department: Informs the RASSU department about any change of Drug Law/guidelines and updated requirements for submission on the country level
Wolters Kluwer is a global leader in professional information services that combines deep domain knowledge with specialized technology. Our portfolio offers software tools coupled with content and services that customers need to make decisions with confidence.
Company Description Medicine moves forward here. So will you. At PrimeVigilance, patient safety is not one part of the job. It is why we exist. We are a global pharmacovigilance specialist. Our teams help clients navigate
At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and
SOLTI is an academic research group that performs clinical trials of excellence in oncology. Currently, SOLTI is comprised of over 550 renowned research professionals distributed over a broad network of more than 100 leading hospitals in
Company Description Medicine moves forward here. So will you. At PrimeVigilance, patient safety is not one part of the job. It is why we exist. We are a global pharmacovigilance specialist. Our teams help clients navigate
Medical Information Associate Dutch Language Full-time Department: PV Medical Information Medicine moves forward here. So will you. At PrimeVigilance, patient safety is not one part of the job. It is why we exist. We are a global
Are you an experienced Regulatory Affairs professional who enjoys taking ownership, challenging existing ways of working and turning regulatory expertise into practical improvements? Would you like to work across Southern European markets while helping colleagues and
Position: Regulatory Affairs Associate – Temporary (maternity leave) Location: Madrid (on-site) Experience: 3+ years Want to know more? Exeltis is a pharmaceutical company committed to improving people’s health and well‑being through the development, manufacturing, and commercialization of
Location: Spain (Madrid or Barcelona based) Who we are? Optimapharm is a mid-sized, global Contract Research Organisation turning science into hope through agile, patient-focused clinical development. At Optimapharm, youll have the opportunity to work on diverse
Responsibilities Asegúrese de leer detenidamente la información sobre esta oportunidad antes de presentar su candidatura. Acquire and maintain parallel trading licenses, including dossier preparation, submissions, and lifecycle management Prepare and proofread packaging materials, artwork files, mock-ups,
Optimapharm is seeking a CRA in Spain (Madrid/Barcelona based) to perform routine site visits, monitor trials, and ensure data integrity across studies. Requirements include a medical/pharmacy degree and at least 4 years of independent monitoring experience, with
Location: Spain (Madrid or Barcelona based)Who we are? Optimapharm is a mid-sized, global Contract Research Organisation turning science into hope through agile, patient-focused clinical development. At Optimapharm, you’ll have the opportunity to work on diverse and
In a nutshell Los candidatos deben tomarse el tiempo de leer atentamente todos los elementos de este anuncio de empleo. Por favor, envíen su solicitud sin demora. Position: Regulatory Affairs Associate – International Markets Location: Madrid Experience:
Responsibilities Acquire and maintain parallel trading licenses, including dossier preparation, submissions, and lifecycle management Prepare and proofread packaging materials, artwork files, mock-ups, item lists, and regulatory documentation Communicate with competent authorities and stakeholders across assigned markets
Job Title Clinical Specialist Iberia Surgery (Field) Desplácese hacia abajo para obtener una visión general completa de lo que requerirá este trabajo. ¿Es usted el candidato adecuado para esta oportunidad? Location BD in San Agustín de
TakeTalent joins PharmaMar i n the search for a Clinical Pharmacology Scientist to support the development of innovative oncology therapies through cutting-edge clinical pharmacology and model-informed drug development strategies . At PharmaMar , they are committed
Company Description Medicine moves forward here. So will you. At PrimeVigilance, patient safety is not one part of the job. It is why we exist. We are a global pharmacovigilance specialist. Our teams help clients navigate
Job Description Role and Responsibilities The Manager, Commercial Quality is responsible for leading and overseeing Quality operations across the Ergomed Group. Responsibilities include management, upkeep, and delivery of Quality Cost Grids, Quality as a Service information