Senior Clinical Research Nurse Coordinator for Madrid Trials

hace 3 días


Zaragoza, Zaragoza, España Course A tiempo completo

Job Title: Senior Clinical Research Nurse Coordinator for Madrid Trials

About IQVIA:

IQVIA is a leading company in the clinical research industry, offering a dynamic and challenging work environment.

Estimated Salary:

$65,000 - $85,000 per year, depending on experience.

About the Job:

We are seeking an experienced Clinical Research Nurse Coordinator to join our team in Madrid. As a key member of our site team, you will be responsible for supporting clinical research studies and maintaining a safe study environment according to health and safety policies under the direction and delegation of the Principal Investigator.

You will perform patient vital signs, ECGs, and blood withdrawals, safeguard the well-being of subjects, act as a volunteer advocate, and address subjects' concerns. You will also maintain up-to-date study protocols, case report forms (CRFs), Electronic Data Capture (EDC) systems, and other study documents.

Key responsibilities include planning and coordinating logistical activity for study procedures according to the study protocol, performing clinical set-up and preparation for the study, and assisting with data entry, data quality checking, and query resolution to ensure adherence to study protocol and quality control for content accuracy and completeness.

Additional responsibilities include assisting 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, and coordinating with study monitor on study issues and effectively responding to monitor-initiated questions.

Requirements:

To be successful in this role, you will need a BS/BA in life sciences or an educational equivalent and/or relevant work experience in a clinical environment or medical setting, such as a clinical research coordinator, nurse, medical assistant, or other medical profession.

You will also require experience performing patient vital signs, ECGs, and blood withdrawals, 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, and strong IT competence, skilled in using MS Windows and Office applications such as Access, Outlook, Excel, and Word.

Working with Us:

We offer a dynamic and supportive work environment, competitive salary, and opportunities for professional growth and development.

Contact Information:



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