CALL FOR APPLICATIONS FOR THE EMPLOYMENT OF A UNIVERSITY GRADUATE FOR THE POSITION OF PHYSICIAN[...]

European Commission; Castellón de la Plana; Presencial; EUR 40.000 - 55.000; Jornada completa

Descripción de la vacante

La Comisión Europea busca un investigador para gestionar ensayos clínicos de vacunas en Castellón de la Plana. Este puesto requiere una sólida formación en Medicina y experiencia comprobada en ensayos clínicos, junto con habilidades avanzadas en gestión y organización para garantizar el éxito de los estudios. Se ofrece un contrato a tiempo completo y la necesidad de una firma electrónica para el contrato laboral.

Formación

• Experiencia de al menos 2 años en ensayos clínicos con vacunas.
• Curso de Soporte Vital Avanzado.
• Experiencia en unidades de ensayos clínicos.

Responsabilidades

• Gestión de ensayos clínicos de vacunas.
• Participación en la selección de sujetos.
• Realización de historias clínicas y exámenes físicos.

Conocimientos

Experiencia en ensayos clínicos

Conocimiento de plataformas de ensayos clínicos

Formación en investigación clínica

Educación

Grado en Medicina

Descripción del empleo

Organisation / Company Fundación Investigación Biomédica del Hospital de la Princesa Research Field Medical sciences » Other Researcher Profile Recognised Researcher (R2) Positions Bachelor Positions Country Spain Application Deadline 18 Jun 2025 - 23 : 59 (Europe / Madrid) Type of Contract To be defined Job Status Full-time Is the job funded through the EU Research Framework Programme? Not funded by a EU programme Reference Number 31 / 2025 Is the Job related to staff position within a Research Infrastructure? No

Offer Description

REQUIREMENTS

Candidates must provide the required qualification.

EDUCATION

• Degree in Medicine

EXPERIENCE

• Experience in the development of bioequivalence clinical trials.
• At least 2 years of experience conducting clinical trials with vaccines.
• Experience in coordination, initiation, organization, and management of clinical trials with healthy volunteers and patients.
• Advanced Life Support course.

OTHER REQUIREMENTS

• Work experience in Clinical Trial Units with vaccines.
• Courses related to Clinical Research
• Courses related to Pharmacovigilance
• Knowledge of platforms related to clinical trials : randomization systems, CRDs, patient management systems.

EXPERIENCE

• Experience in the development of bioequivalence clinical trials.
• At least 2 years of experience conducting clinical trials with vaccines.
• Experience in coordination, initiation, organization, and management of clinical trials with healthy volunteers and patients.
• Advanced Life Support course.

OTHER REQUIREMENTS

• Work experience in Clinical Trial Units with vaccines.
• Courses related to Clinical Research
• Courses related to Pharmacovigilance
• Knowledge of platforms related to clinical trials : randomization systems, CRDs, patient management systems.

TASKS TO BE PERFORMED

• Responsible for the management of vaccine clinical trials.
• Participation in subject screening tasks.
• Conducting medical histories and physical examinations of healthy volunteers.
• Interpretation of ECGs and laboratory tests.
• Recording of adverse events.

Additional Information

Eligibility criteria

Evaluation Criteria :

The evaluation criteria for this offer are as follows up to a maximum of 11 points :

• Work experience in vaccine clinical trial units : 0.1 points per month worked, up to a maximum of 2 points
• Courses related to clinical research : 0.2 points per course, up to a maximum of 1 point
• Experience with clinical trial platforms : 1 point per platform
• Courses related to pharmacovigilance : 1 point
• Personal interview : up to 5 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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