Contractor Cra_Spain

Tigermed; Navarra; Presencial; EUR 55.000 - 75.000; Jornada completa

Descripción de la vacante

Tigermed, situado en Navarra, España, busca un CRA con experiencia para gestionar sitios, realizar monitorización y asegurar el cumplimiento de GCP y del protocolo. Se espera coordinación de materiales, formación continua y gestión de la seguridad de los ensayos clínicos.

Las responsabilidades incluyen control de documentos, finanzas y sistemas, y la entrega de informes puntuales con seguimiento de reclutamiento. Se valorará experiencia en SAE y manejo de herramientas de oficina.

Formación

• Bachelor degree or above in Medical, Pharmacology or Biology related major.
• At least 8 year of CRA experience.
• Good understanding and knowledge of Good Clinical Practice and clinical trial operation processes.
• Good skills on Microsoft Word, Excel, PPT and Outlook, etc.

Responsabilidades

• Site management including study site selection, initiation (SIV) and clinical monitoring.
• Conduct monitoring visits according to SDV plan and SOP; address issues with sites.
• Ensure safety information is disseminated to all sites and SAE reporting within timeline.
• Finalize budget and obtain signed contract from site prior to initiation visit.
• Ensure Study Payment Schedule is executed and retain relevant documents/receipts.
• Update and maintain Study tools/systems in a timely manner.

Conocimientos

GCP knowledge

Trial operations

Microsoft Word

Microsoft Excel

PowerPoint

Outlook

Educación

Bachelor degree or above in Medical, Pharmacology or Biology related major

Herramientas

Microsoft Word

Microsoft Excel

PowerPoint

Outlook

Descripción del empleo

Descripción del trabajo

Responsibilities

Asegúrese de leer detenidamente la información sobre esta oportunidad antes de presentar su candidatura.

(a) Site management

Study site selection, initiation (SIV) and clinical monitoring.

Perform pre-study visit to ensure eligible sites are selected according to sponsor site selection criteria, including but not limited to adequate resources and experience.

Prepare and conduct SIV to ensure adequate study training for relevant site staff to proceed with study start and conduct in compliance with protocol and relevant regulations.

Ensure Principal Investigator/study staff complies with safety reporting requirements, as defined in protocol, SOP, ICH-GCP and GCP.

Track study recruitment to ensure recruitment target is achieved in all studies.

Conduct monitoring visit according to SDV plan and SOP; address issues with sites and complete monitoring visit report in a timely manner coordinating.

Ensure timely coordination of study materials (drug, non-drug, equipments, CRFs) to the site for start-up and throughout the study.

Assemble site specific EC submission dossier, and ensure submission to EC.

Training

Provide ongoing training to site staff with regards to ICH-GCP, GCP, study protocol and requirements.

Conduct site initiation to ensure that the site has a thorough understanding of the study protocol and requirements.

Documentation

Ensure timely collection of essential documents in compliance with protocol and regulations at study start-up, during and at study close-down. Maintain and update these documents in investigator files, trial master files.

Prepare/complete study records' archiving according to protocol and sponsor requirements.

(b) Drug Safety

Ensure safety information is disseminated to all sites according SOP and applicable regulations.

Ensure SAE is reported within the timeline in compliance with SOPs and applicable regulations.

(c) Finance and Administration

Finalize budget and obtain signed contract from site, prior to site initiation visit.

Ensure Study Payment Schedule is executed and retain relevant documents/receipts.

(d) Study Tools and system

Update and maintain Study tools/systems in a timely manner. xkdbapo

3. Qualifications

• 3.1 Bachelor degree or above in Medical, Pharmacology or Biology related major.
• 3.2 At least 8 year of CRA experience;
• 3.3 Good understanding and knowledge of Good Clinical Practice and clinical trial operation processes/procedures;
• 3.4 Good skills on Microsoft Word, Excel, PPT and Outlook, etc.