Organisation / Company: IDIVAL
Department: Human Resources Department
Research Field: Medical sciences > Health sciences
Researcher Profile: Recognised Researcher (R2)
Positions: Master Positions
Country: Spain
Application Deadline: 29 Jun 2025 - 23:59 (Europe / Brussels)
Type of Contract: Permanent
Job Status: Full-time
Hours Per Week: 35
Offer Starting Date: 20 Jun 2025
Funding: Not funded through the EU Research Framework Programme
Research Infrastructure Staff Position: No
Offer Description

Academic Degree:

Bachelor's degree + Official Master's degree / equivalent (must be justified with the application).
Functions:
Monitor clinical trial activities at assigned sites as defined by the project manager.
Ensure effective communication between investigators and the promoter team.
Conduct kick-off visits and train research teams.
Carry out monitoring in accordance with the Monitoring Plan and manual.
Verify protocol compliance and modifications.
Ensure adherence to Good Clinical Practice guidelines and applicable legislation.
Conduct clinical trial closure visits.
Prepare monitoring and review reports.
Maintain up-to-date trial documentation at sites.
Support resolution of data inconsistencies, deviations, and errors.
Ensure traceability of medication delivery.
Maintain information in project monitoring tools.
Collaborate in quality assurance of data and processes.
Produce periodic reports in English.
Assist in product materiovigilance reports.
Qualifications:
Master in Clinical Trials or Master in Health Care Research.
Good Clinical Practice Certification.
Experience in monitoring clinical trials, pharmacovigilance, or materiovigilance management.
Experience as Data Manager or Study Coordinator.
English B2 or higher.
Driving license B.
Additional Requirements:
Academic degree as above.
Salary:

26,717.29€ gross annually, subject to updates in legislation for 2024.
Eligibility Criteria

Master in Clinical Trials or Health Care Research (Maximum 15 points).
Good Clinical Practice Certification (Maximum 10 points).
Experience in clinical trial monitoring or pharmacovigilance (Maximum 15 points).
Experience as Data Manager or Study Coordinator (Maximum 10 points).
English B2 or higher (Maximum 5 points).
Driving license B (Maximum 5 points).
Selection Process

Application submission.
Competition phase.
Interview with up to 3 candidates; minimum score for interview: 30 points.
Report of the Tribunal.
Final resolution.
Note: Candidates must score at least 30 points to be considered for recruitment and employment exchange purposes.

#J-18808-Ljbffr