Remote Health Monitoring / Telecare Sales – Spain

Chronos Consulting; Torrejón de Ardoz; A distancia; EUR 20.000 - 30.000; A tiempo parcial

Descripción de la vacante

A leading company in clinical research is seeking a Clinical Research Coordinator to support various administrative tasks and ensure smooth clinical trial operations. This part-time position (24 hours/week) requires a BS/BA in life sciences and relevant experience. The successful candidate will contribute to volunteer recruitment and study monitoring while maintaining protocols and quality standards.

Formación

• Relevant work experience in a clinical environment or medical setting preferred.
• In-depth knowledge of departmental and study-specific procedures.
• Entry-level position.

Responsabilidades

• Support clinical research studies, ensuring adherence to study protocols.
• Maintain study documentation and assist with data quality checking.
• Coordinate logistical activities for study procedures.

Conocimientos

Interpersonal skills

Organization

Attention to detail

IT competence

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 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 :

• 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 subjects’ 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, or 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 clients.
• 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

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