CALL FOR APPLICATIONS FOR THE HIRING OF A SENIOR DEGREE HOLDER FOR THE POSITION OF CLINICAL TRI[...]

European Commission; Sevilla; Presencial; EUR 30.000 - 50.000; Jornada completa

Descripción de la vacante

La Comisión Europea busca un Coordinador de ensayos clínicos con enfoque en Dermatología en Sevilla. El candidato será responsable de colaborar en ensayos clínicos, gestionar documentos y mantener registros, así como participar en auditorías. Se requiere experiencia previa en investigación clínica y un alto nivel de inglés.

Formación

• Experiencia mínima de 6 meses como Coordinador en Dermatología.
• Formación en Buenas Prácticas Clínicas (GCP).
• Certificación IATA para manejo de muestras biológicas.

Responsabilidades

• Colaborar en ensayos clínicos y proyectos de investigación.
• Gestión de documentación de ensayos clínicos.
• Participar en auditorías relacionadas.

Conocimientos

Colaboración

Resolución de consultas

Análisis crítico

Comunicación efectiva

Educación

Grado Universitario en Ciencias de la Salud

Máster en Monitoreo y Coordinación de Ensayos Clínicos

Descripción del empleo

Organisation / Company Fundación Investigación Biomédica del Hospital de la Princesa Research Field Medical sciences » Health sciences Researcher Profile Recognised Researcher (R2) Positions Master Positions Country Spain Application Deadline 4 Jul 2025 - 23 : 59 (Europe / Madrid) Type of Contract Temporary Job Status Full-time Is the job funded through the EU Research Framework Programme? Not funded by a EU programme Reference Number 41 / 2025 Is the Job related to staff position within a Research Infrastructure? No

Offer Description

REQUIREMENTS

a) EDUCATION

• Higher University Degree in the Health Sciences field (Biology, Pharmacy, Biotechnology, Nursing, Veterinary Medicine, etc.).
• Master’s Degree in Clinical Trial Monitoring and Coordination.

b) EXPERIENCE

• Previous experience as a Coordinator in Dermatology. A minimum of 6 months of experience is required in clinical trials on psoriasis, atopic dermatitis, cutaneous lupus, hidradenitis suppurativa, and chronic urticaria.
• Minimum of 6 months prior experience in Pharmacovigilance.
• Minimum of 6 months prior experience in clinical research projects on dermatological diseases.

c) OTHER REQUIREMENTS

• Training in Good Clinical Practice (GCP).
• Certified training in the handling of biological samples (IATA certification required).
• High level of English language proficiency (C1 or higher), accredited by an official valid certificate.

EDUCATION

• Higher University Degree in the Health Sciences field (Biology, Pharmacy, Biotechnology, Nursing, Veterinary Medicine, etc.).
• Master’s Degree in Clinical Trial Monitoring and Coordination.

Specific Requirements

EXPERIENCE

• Previous experience as a Coordinator in Dermatology. A minimum of 6 months of experience is required in clinical trials on psoriasis, atopic dermatitis, cutaneous lupus, hidradenitis suppurativa, and chronic urticaria.
• Minimum of 6 months prior experience in Pharmacovigilance.
• Minimum of 6 months prior experience in clinical research projects on dermatological diseases.

OTHER REQUIREMENTS

• Training in Good Clinical Practice (GCP).
• Certified training in the handling of biological samples (IATA certification required).
• High level of English language proficiency (C1 or higher), accredited by an official valid certificate.

TASKS TO BE PERFORMED

• Collaborate in clinical trials and research projects conducted within the Department.
• Data entry and resolution of queries.
• Review of medical records to extract all necessary medical information for the Dermatology Department’s research projects.
• Participation in National Registries of dermatological diseases.
• Collaboration in the Pharmacovigilance System conducted by the Spanish Agency of Medicines and Medical Devices (AEMPS), coordinated by the Spanish Academy of Dermatology and Venereology.
• Maintenance and management of documentation related to National Registries and clinical trials.
• Participation in and cooperation with any audits.

Additional Information

Eligibility criteria

Evaluation Criteria :

The evaluation criteria for this offer are as follows up to a maximum of 24 points :

• Previous experience as a Dermatology Clinical Trial Coordinator : up to 6 points.
• Prior experience in Pharmacovigilance : up to 4 points.
• Previous experience in clinical research in Dermatology : up to 4 points.
• GCP certificate : 1 point.
• IATA certificate for handling biological samples : 1 point.
• English language proficiency certified at : C1 : 1 point, C2 : 2 points
• Personal interview : up to 6 points.

Selection process

Applications that meet the requirements and are within the call's deadline will be reviewed by a jury composed of three members (a president and two members).

A curriculum evaluation will be conducted for the received applications, and points will be assigned based on the merits presented, according to the job requirements.

Subsequently, candidates may be called for a personal interview.

Additional comments

EQUAL OPPORTUNITIES FOR WOMEN AND MEN

In equal conditions of suitability, capacity, and merits, preference will be given to the hiring of the gender less represented in the group in question.

Please note that the use of a single gender in this document is intended to facilitate readability and avoid duplicating articles, nouns, and adjectives in both masculine and feminine forms.

MANDATORY ELECTRONIC SIGNATURE

The selected candidate must have an electronic signature, which is a mandatory requirement for signing the employment contract.

Work Location(s)

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