Trabajo Clinical Research - Barcelona

Postdoctoral Researcher in Innate Immune Biology (ref. PD/23/14) Created in 2005 by the Generalitat de Catalunya (Government of Catalonia) and the University of Barcelona, IRB Barcelona is a Severo Ochoa Centre of Excellence—a seal that was awarded in 2011. The institute is devoted to conducting res...

The Associate Director – Regulatory Submissions The Associate Director – Regulatory Submissions is responsible to lead a worldwide Regulatory Submissions delivery team within IQVIA Translations. This team is in charge of the development and harmonization of the Regulatory Submissions Process. The As...

[Hw-] - Rf- Corporate Accounts Manager Spain F-728 Barcelona, Catalonia [Hw-] - Rf- Corporate Accounts Manager Spain F-728 Barcelona Barcelona, Catalonia, ES . Life Unlimited. At Smith+Nephew we design and manufacture technology that takes the limits off living. Smith+Nephew 's Corporate Account Man...

Título del puesto: Codificador/a de Documentación Médica Descripción del puesto: Estamos buscando un/a Codificador/a de Documentación Médica calificado/a para unirse a nuestro equipo como freelance o autónomo para trabajar de forma remota. Responsabilidades: Codificar documentación clínica en CIE-10...

Job Description Take your career to the next level and lead challenging full-service global clinical research projects, managing the full scope of responsibilities and getting hands-on involvement in every aspect of the study. Your responsibilities will include: Management of global, multi-center cl...

As a Clinical Research Associate (CRA) you will coordinate all aspects of the clinical monitoring and site management process in accordance with regulatory guidelines, local regulations and standard operating procedures. In this role you will be a decision maker, solving problems independently or as...

Molecular Nanoscience and Organic Materials Department, NANOMOL-BIO group ( https://icmab.es/mnom/nanomol-bio ); Institut de Ciència de Materials de Barcelona (ICMAB-CSIC). NANOMOL has extensive experience and recognized excellence in the synthesis, processing, and study of molecular and polymeric m...

The Internal Translator is responsible for linguistically and culturally interpreting the written material in a way that maintains or duplicates the structure and style of the original text while keeping the ideas and facts of the original material accurate. They possess fluency in two or more langu...

Home PhD PhD Position in CINC-CSIC, Madrid, Spain PhD Position in CINC-CSIC: Embark on a transformative research journey with the Cognitive Control & Habit Lab at CINC-CSIC, located in Alcala de Henares, Madrid, Spain. This PhD position, titled “The role of habitual inhibition in cognitive and emoti...

Requisition Number6390Employment Type : Regular Who we are Worldwide Clinical Trials (Worldwide), a leading global contract research organization (CRO), works in partnership with biotechnology and pharmaceutical companies to create customized solutions that advance new medications from discovery to ...

Description JOB FUNCTION : Primarily focused on providing technical support in activities related to the development and implementation of local Studies for the generation of data in epidemiology and Real World Evidence studies (RWE). Maintain knowledge in legislation and local regulation for doing ...

For more than 75 years, Grifols has worked to improve the health and well-being of people around the world. We are a global healthcare company that produces essential plasma-derived medicines for patients and provides hospitals and healthcare professionals with the tools, information and services th...

Direct to Participants Product Owner Location : flexible across Europe, home based Direct to Participants (DTP) Product Owner provides expertise and system support in developing and enhancing the participant portal of the Health Research Space (HRS) product. The participant portal is expected to be ...

Job Overview Manage and support the operational elements and execution of studies and / or programs to ensure delivery; time and quality resulting in strong financial performance and customer satisfaction and in accordance with SOPs; policies and practices from pre-award to close-out. Work with stud...

Perform daily administrative activities, in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams, to ensure a complete and accurate Trial Master File delivery. Essential Functions Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team with ac...