AIM The Vall d’Hebron University Hospital makes its own and open call for the recruitment of Health Professionals Affiliated with the Nursing Directorate. OBJECTIVE To facilitate the dedication to research of two professionals in Nursing, Midwifery, Physiotherapy, Occupational Therapy,
Site monitoring and site management responsibility for clinical studies according to Company, and/or Sponsor, Standard Operating Procedures, and Regulatory Guidelines. Assures the implementation of project plans, as assigned. Summary of Responsibilities: Responsible for all aspects of
Site monitoring and site management responsibility for clinical studies according to Company, and/or Sponsor, Standard Operating Procedures, and Regulatory Guidelines. Assures the implementation of project plans, as assigned. Summary of Responsibilities: Responsible for all aspects of
Who we are We’re a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world’s most persistent diseases is not paved by those who play it safe. It
Company Description About AbbVie AbbVies mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on
The Barcelona Institute for Global Health (ISGlobal) is a cutting-edge institute addressing global public health challenges through research, translation into policy and education. ISGlobal has a broad portfolio in communicable and non-communicable diseases including environmental and climate
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
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
When our values align, theres no limit to what we can achieve. At Parexel, we all share the same goal - to improve the worlds health. From clinical trials to regulatory, consulting, and market access, every
Join us in redefining what it means to work for a CRO. When you work at Rho, it’s more than just a job—you become part of the Rho Factor. We’re a proud bunch of science nerds
Description Start-Up Manager, EU, remote: Poland, Spain or Germany The Start-Up Manager is responsible for overseeing and managing the successful and timely activation of clinical trial sites across multiple countries. This role leads all start-up activities,
Work ScheduleStandard (Mon-Fri) Environmental ConditionsOffice Job Description Competitive sign-on bonus considered for qualified candidates Join Us as a Clinical Research Associate! – Make an Impact at the Forefront of Innovation Were hiring CRA (Level II) to Sr
VHIR is offering a position for a Laboratory Technician to join the Clinical Research Support Unit (USIC). The role will primarily involve technical laboratory activities related to the processing, storage and shipment of human biological samples, together
Veeva Systems is a mission-driven organization and pioneer in industry cloud, helping life sciences companies bring therapies to patients faster. As one of the fastest-growing SaaS companies in history, we surpassed $3B in revenue in our
Description Start-Up Manager, Canada, remote: The Start-Up Manager is responsible for overseeing and managing the successful and timely activation of clinical trial sites across multiple countries. This role leads all start-up activities, ensures regulatory compliance, and
START Center for Cancer Research (START) is the worlds largest network of Phase I clinical trial centers, dedicated exclusively to oncology research. Since its inception, START has provided hope to cancer patients across global communities by offering access
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 Spain, Portugal,
Overview In this role you will oversee and drive the conduct of clinical trials to ensure alignment with protocol, GCP, and regulatory standards. You will monitor sites, manage data integrity, and support cross-functional teams to enable
ICON plc is a world‑leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of
Please consider the following before applying: Envíe su solicitud a continuación después de leer todos los detalles y la información de apoyo sobre esta oportunidad de trabajo. The internship will start in September 2026. You need