Job Search and Career Advice Platform

¡Activa las notificaciones laborales por email!

Clinical Research Coordinator - Madrid

IQVIA

Madrid

Presencial

EUR 30.000 - 45.000

Jornada completa

Hace 16 días

Genera un currículum adaptado en cuestión de minutos

Consigue la entrevista y gana más. Más información

Descripción de la vacante

A leading clinical research company in Madrid is seeking a Clinical Research Coordinator to support clinical trials and ensure smooth operations. The ideal candidate will have a BS/BA in life sciences or equivalent, along with experience in a clinical setting. Responsibilities include maintaining study protocols, assisting with subject recruitment, and monitoring quality control. Strong IT skills and excellent organizational abilities are essential. This position provides a fantastic opportunity to contribute to innovative medical treatments.

Formación

  • BS / BA in life sciences or equivalent required.
  • Relevant work experience in a clinical environment is preferred.
  • Basic knowledge of clinical trials and procedures needed.

Responsabilidades

  • Support clinical research studies and maintain study environments.
  • Recruit, screen, and orient volunteers according to protocols.
  • Maintain up-to-date study protocols and documentation.

Conocimientos

Strong IT competence
Excellent interpersonal skills
Good organizational skills
Basic knowledge of medical terminology

Educación

BS / BA in life sciences or equivalent

Herramientas

MS Windows
MS Office (Access, Outlook, Excel, Word)
Descripción del empleo

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 are looking for a Clinical Research Coordinator.

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 :

  • 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
  • Safeguard the well-being of subjects, act as a volunteer advocate, and address subject’s concerns
  • Maintain up-to-date study protocols, case report forms (CRFs), Electronic Data Capture (EDC) systems, and other study documents
  • Plan and coordinate logistical activity for study procedures according to the study protocol
  • 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
  • Assist with data entry, data quality checking, and query resolution to ensure adherence to study protocol and quality control for content accuracy and completeness
  • Assist in study enrollment by recruiting, screening, and orienting volunteers according to the study protocol
  • Correct custody of study drug according to site standard operating procedures
  • 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 :

  • 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, other medical profession
  • Basic knowledge of clinical trials, combined with in-depth knowledge of departmental, protocol and study-specific operating procedures, consent forms, and study schedules
  • Basic knowledge of medical terminology
  • Strong IT competence, skilled in using MS Windows and Office applications such as Access, Outlook, Excel, and Word
  • Excellent interpersonal skills with the ability to establish and maintain effective working relationships with co-workers, managers and client
  • Good organizational skills with the ability to pay close attention to detail.

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at

Consigue la evaluación confidencial y gratuita de tu currículum.
o arrastra un archivo en formato PDF, DOC, DOCX, ODT o PAGES de hasta 5 MB.