Última información laboral de Thermo Fisher Scientific para la posición de Cra I/ Ii- Fsp. If the Cra I/ Ii- Fsp vacante en Madrid coincide con tus calificaciones, envía tu solicitud o currículum directamente a través del portal actualizado de Jobkos.
Ten en cuenta que aplicar a un trabajo puede no ser siempre fácil, ya que los candidatos deben cumplir con ciertos requisitos establecidos por la empresa. Esperamos que esta oportunidad en Thermo Fisher Scientific para la posición de Cra I/ Ii- Fsp se ajuste a tu perfil profesional.
Work Schedule
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Job Description
Ready to take the Sig step in your CRA career?
At CRG Thermo Fisher Scientific, we are offering an exciting opportunity to join a dedicated partnership with a leading global pharmaceutical Empresa — giving you the chance to grow your career in a dynamic, client-dedicated environment.
Are you an Assistant / In House CRA looking to become a CRA? Do you already have 1–2 years of CRA experience and want to broaden your experience within a client-dedicated model? Are you looking for a Empresa where you can continue learning, growing, and building a long-term career?
We are hiring both Junior and experienced CRAs who are passionate about clinical research and eager to work on innovative studies while being supported by a global organization committed to career development and internal growth.
At Thermo Fisher Scientific, you won’t just join a Empresa — you’ll join a team that invests in your future.
Ready for your Sig challenge?
Join Us as a Clinical Research Associate – Make an Impact at the Forefront of Innovation. You will be fully dedicated to one of our clients.As part of our global team, you’ll have the opportunity to perform and coordinate all aspects of the clinical monitoring and site management process. As a Clinical Research Associate, you'll conduct remote or on-site visits to assess protocol and regulatory compliance and manage required documentation. You will manage procedures and guidelines from different sponsors and/or monitoring environments (i.E., FSO, FSP, Government, etc.). Acting as a site processes specialist, you will ensure that the trial is conducted in accordance with the approved protocol, ICH-GCP guidelines, applicable regulations, and SOPs to guarantee subjects' rights, well-being, and data reliability. You will ensure audit readiness and develop collaborative relationships with investigational sites. Detailed tasks and responsibilities assigned to your role are outlined in the task matrix.What You’ll Do: - Monitors investigator sites with a risk-based monitoring approach: applies root cause analysis (RCA), critical thinking and problem-solving skills to identify site processes failure and corrective/preventive actions to bring the site into compliance and decrease risks. Ensures data accuracy through SDR, SDV and CRF review as applicable through on-site and remote monitoring activities. Assess investigational product through physical inventory and records review. Documents observations in reports and letters in a timely manner using approved business writing standards. Escalates observed deficiencies and issues to clinical management expeditiously and follow all issues through to resolution. May need to maintain regular contact between monitoring visits with investigative sites to confirm that the protocol is being followed, that previously identified issues are being resolved and that the data is being recorded in a timely manner. Conducts monitoring tasks in accordance with the approved monitoring plan. Participates in the investigator
Información de la Vacante:
Empresa: Thermo Fisher Scientific
Puesto: Cra I/ Ii- Fsp
Lugar de Trabajo: Madrid
País: ES
Cómo Enviar tu Postulación:
Después de leer y comprender los criterios y requisitos mínimos explicados en la información del trabajo Cra I/ Ii- Fsp at the office Madrid anterior, completa de inmediato tus archivos de solicitud, como carta de presentación, CV (Hoja de Vida), copia de diploma y otros suplementos. Envía a través del enlace Siguiente Página abajo.
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