Research Support Technician (2025.37)

Euraxess; Sevilla; Presencial; EUR 27.000; Jornada completa

Descripción de la vacante

A leading organization in research is seeking a Recognised Researcher for full-time roles in clinical trial monitoring within Sevilla, Spain. The selected candidate will support clinical activities by ensuring compliance with protocols, effective communication, and high-quality data management. Applicants should hold a Master's in Clinical Trials and have relevant experience in monitoring processes. This position promises to offer a challenging and rewarding career in health research, with applications due by May 30, 2025.

Formación

• Master in Clinical Trials / Clinical Trial Monitoring required.
• Good Clinical Practice Certification essential.
• Experience as Data Manager or Study Coordinator is preferred.

Responsabilidades

• Monitor clinical trial activities and ensure communication between teams.
• Conduct training for research teams and prepare Monitoring Reports.
• Ensure compliance with guidelines and maintain site documentation.

Conocimientos

Clinical Trial Monitoring

Good Clinical Practice Certification

Communication

Educación

Master in Clinical Trials

Descripción del empleo

Researcher Profile : Recognised Researcher (R2)

Positions : Master Positions

Country : Spain

Application Deadline : 30 May 2025 - 23 : 59 (Europe / Brussels)

Type of Contract : Permanent

Job Status : Full-time

Offer Starting Date : 21 May 2025

Is the job funded through the EU Research Framework Programme? Not funded by a EU programme

Is the Job related to staff position within a Research Infrastructure? No

Offer Description

Academic Degree

• Bachelor's degree + Official Master's degree / equivalent (must be provided with the application).

Functions

• Monitor clinical trial activities at assigned sites as defined by the project manager.
• Ensure effective communication between the investigator / promoter team at the sites.
• Conduct start-up visits and train research teams.
• Carry out monitoring in accordance with the Monitoring Plan and manual.
• Verify compliance with protocol and modifications.
• Ensure adherence to Good Clinical Practice guidelines, legislation, and SOPs.
• Conduct clinical trial closure visits.
• Prepare Monitoring and Review Reports for the project manager / promoter.
• Maintain accurate and up-to-date documentation at sites.
• Assist in resolving data inconsistencies, deviations, and errors.
• Ensure traceability of medication delivered.
• Maintain monitoring tools with site information.
• Collaborate in quality assurance of data, documentation, and processes.

Qualifications

• Master in Clinical Trials / Clinical Trial Monitoring
• Good Clinical Practice Certification
• Experience in Clinical Trial Monitoring
• Experience as Data Manager or Study Coordinator in Clinical Trials
• English B2 or higher
• Driving licence B

Additional Information

Annual Gross Salary : 26,717.29 € (subject to legislative updates for 2024)

Eligibility Criteria

• Master in Clinical Trials / Clinical Trial Monitoring (max 15 points)
• Good Clinical Practice Certification (max 10 points)
• Experience in Clinical Trial Monitoring (max 15 points)
• Experience as Data Manager or Study Coordinator (max 10 points)
• English B2 or higher (max 5 points)
• Driving licence B (max 5 points)

Selection Process

• Application submission
• Competition phase
• Interview : up to 3 candidates; minimum score : 40
• Report of the Tribunal
• Final resolution

Note : Candidates need at least 30 points to be considered for employment.

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