Remote Health Monitoring / Telecare Sales – Spain

Chronos Consulting; Santander; A distancia; EUR 20.000 - 35.000; A tiempo parcial

Descripción de la vacante

A leading industry player seeks an experienced Clinical Research Coordinator for part-time work in Valencia. The role involves supporting clinical trials and ensuring compliance with protocols. Ideal candidates will have a degree in life sciences alongside relevant clinical experience. Strong organizational and interpersonal skills are essential for success in this dynamic environment.

Formación

• Entry-level position, relevant experience in clinical environment preferred.
• Basic knowledge of clinical trials and medical terminology essential.
• Strong IT skills; proficiency in MS Office required.

Responsabilidades

• Support clinical research studies and maintain study environment.
• Assist with patient recruiting, data entry, and quality checking.
• Coordinate logistical activities for study procedures.

Conocimientos

Interpersonal skills

Organizational skills

IT competence

Knowledge of medical terminology

Educación

BS / BA in life sciences

Herramientas

MS Windows

MS Office applications

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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