Gestor / A De Tripulaciones

Altia; Madrid; Presencial; EUR 30.000 - 50.000; A tiempo parcial

Descripción de la vacante

Una empresa líder en la industria busca un Coordinador de Investigación Clínica para un emocionante proyecto en Valencia. Esta posición de medio tiempo es ideal para aquellos con una formación en ciencias de la vida y experiencia en entornos clínicos. El candidato seleccionado desempeñará un papel clave en el apoyo a los investigadores, asegurando el cumplimiento de los protocolos de estudio y la calidad de los datos. Si te apasiona la investigación clínica y quieres contribuir a la mejora de la atención médica, esta es una oportunidad perfecta para ti.

Formación

• Experiencia en un entorno clínico o médico como coordinador de investigación clínica o enfermero.
• Conocimientos de procedimientos operativos específicos de estudios y formularios de consentimiento.

Responsabilidades

• Apoyar estudios de investigación clínica y mantener un entorno seguro según políticas de salud.
• Mantener protocolos de estudio actualizados y realizar la entrada de datos.

Conocimientos

Conocimientos básicos de ensayos clínicos

Terminología médica básica

Competencia informática

Habilidades interpersonales

Organización y atención al detalle

Educación

BS/BA en ciencias de la vida

Herramientas

MS Windows

MS Office (Access, Outlook, Excel, Word)

Descripción del empleo

Job title: Clinical Research Coordinator

Are you looking for an opportunity in Clinical Research? Do you want to work for an industry-leading company? If so, come and join us - IQVIA is looking for an experienced Clinical Research Coordinator for an upcoming project in Valencia on a part-time basis (24 hours per week).

As a pivotal member of the site team, you will be involved with a variety of administrative tasks to support investigators and ensure the smooth running of clinical trials and assist with collecting patient data.

Day-to-day responsibilities will include:

1. Support clinical research studies and maintain a safe study environment according to health and safety policies under the direction and delegation of the Principal Investigator.
2. Safeguard the well-being of subjects, act as a volunteer advocate, and address subjects’ concerns.
3. Maintain up-to-date study protocols, case report forms (CRFs), Electronic Data Capture (EDC) systems, and other study documents.
4. Plan and coordinate logistical activity for study procedures according to the study protocol.
5. Perform clinical set-up and preparation for the study including labeling specimen collection tubes and containers, inventory of required supplies, and setting up or troubleshooting equipment and/or study issues.
6. Assist with data entry, data quality checking, and query resolution to ensure adherence to study protocol and quality control for content accuracy and completeness.
7. Assist in study enrollment by recruiting, screening, and orienting volunteers according to the study protocol.
8. Correct custody of study drug according to site standard operating procedures.
9. Coordinate with study monitor on study issues and effectively respond to monitor-initiated questions.

We are looking for candidates with the following skills and experience:

1. BS/BA in life sciences or educational equivalent and/or relevant work experience in a clinical environment or medical setting, e.g., clinical research coordinator, nurse, medical assistant, or other medical profession.
2. Basic knowledge of clinical trials, combined with in-depth knowledge of departmental, protocol, and study-specific operating procedures, consent forms, and study schedules.
3. Basic knowledge of medical terminology.
4. Strong IT competence, skilled in using MS Windows and Office applications such as Access, Outlook, Excel, and Word.
5. Excellent interpersonal skills with the ability to establish and maintain effective working relationships with co-workers, managers, and clients.
6. Good organizational skills with the ability to pay close attention to detail.

If this sounds like the perfect opportunity for you, apply now!

Seniority level: Entry level

Employment type: Part-time

Job function: Research, Administrative, and Health Care Provider