Clinical Research Coordinator – Toledo (Part-Time, 20-24hours/week) Start Date : immediately Duration : until 30th of September 2026 Antes de solicitar este puesto, por favor, lea la siguiente información sobre esta oportunidad que encontrará a continuación.IQVIA is currently recruiting a dedicated Clinical Research Coordinator to support a clinical research site in Toledo. This part-time...
OverviewWe are working with an exciting US biotech seeking a strategic, dynamic, and highly organized Medical Director to lead and manage international clinical studies focused on an exciting new IVF/IVM product. This role will be pivotal in driving the success of global clinical trials and post-market surveillance studies across key markets including Europe, Australia, the Middle East, Latin...
OverviewResearch Nurse – Decentralized & Hybrid Clinical Trials (Barcelona)Se pueden requerir diversas habilidades interpersonales y experiencia para el siguiente puesto. Por favor, asegúrese de consultar la descripción a continuación con atención.Barcelona, Spain Clinical Research | Patient-Centric Care | Remote & On-Site Operations About the Role A growing clinical research organization in...
We are working with an exciting US biotech seeking a strategic, dynamic, and highly organized Medical Director to lead and manage international clinical studies focused on an exciting new IVF/IVM product. . This role will be pivotal in driving the success of global clinical trials and post-market surveillance studies across key markets including Europe, Australia, the Middle East, Latin America,...
Are you passionate about data integrity, clinical research, and driving excellence through innovation? Join our Biometry team at BCCC and help shape the future of data management in clinical studies.About the RoleAs a Clinical Data Manager, you will play a key role in ensuring the accuracy, integrity, and compliance of clinical study data. You'll collaborate across departments to design and...
Our mission We turn data into better healthcare. With our insights, we make healthcare more affordable, and better, and we improve the patient's and clinicians' experience. Your impact and responsibilities Responsibilities - Project Management: Planning and executing study protocols co-developed by pharmaceutical companies, setting up analyses, and managing projects. This involves proactively...
We are looking for a motivated and detail‐oriented professional to join our clinical team. This role is ideal for someone who enjoys working with patients, supporting clinical operations, and contributing to high‐quality research activities. Se pueden requerir diversas habilidades interpersonales y experiencia para el siguiente puesto. Por favor, asegúrese de consultar la descripción a...
Overview Join Impress – Europe\ 's Leading Health-Tech Innovator! Dé el siguiente paso en su carrera profesional ahora: desplácese hacia abajo para leer la descripción completa del puesto y envíe su solicitud. We believe everyone deserves a smile they\ 'll love. As the largest Ortho clinic chain in Europe, we combine cutting-edge tech with expert care, revolutionizing invisible orthodontics since...
Research Assistant – Pro Pharma (Onsite, 0.6 FTE Lugo) – Start ASAPJoin Pro Pharma, a global leader in clinical research support, as a Research Assistant at our site based in Utrecht. This part-time, 0.6 FTE per-week contract role is a great opportunity to build hands-on experience in clinical research while working in a flexible, supportive environment. .About the role: )As a Research Assistant,...
For one of our international clients we are currently searching forFreelance (Flying) Study Nurse (m/w/d)Background:Adult patients within the broader area of Santiago de Compostela, Spain and Stettin, Poland.Each patient will have 14 Home Visits with Study Nurse Support until ******* (possibility of extension), with approximately 2-3 patients requiring visits in this area. Each visit is expected...
Our mission We turn data into better healthcare. With our insights, we make healthcare more affordable, and better, and we improve the patient's and clinicians' experience. Your impact and responsibilities Responsibilities - Project Management: Planning and executing study protocols co-developed by pharmaceutical companies, setting up analyses, and managing projects. This involves proactively...