Clinical Research Coordinator - Madrid

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 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, as well as 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 wellbeing 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 activities for study procedures according to the study protocol.

Perform clinical setup and preparation for the study, including labeling specimen collection tubes and containers, inventory of required supplies, and setting up or troubleshooting equipment and study issues.

Assist with data entry, data quality checking, and query resolution to ensure adherence to the 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.

Ensure correct custody of study drug according to site standard operating procedures.

Coordinate with study monitor on study issues and respond effectively 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 professions).

Basic knowledge of clinical trials, combined with in-depth knowledge of departmental protocols and study-specific operating procedures, consent forms, and study schedules.

Basic knowledge of medical terminology.

Strong IT skills, including proficiency in MS Windows and Office applications such as Access, Outlook, Excel, and Word.

Excellent interpersonal skills to establish and maintain effective working relationships with coworkers, managers, and clients.

Good organizational skills with close attention to detail.

Additional information such as "LIDNP," "LICES," "LIHCPN," and "LICT1" appears to be internal codes or abbreviations and has been retained as is. The description also includes a general company overview of IQVIA.

The "Required Experience" and "Key Skills" sections mention unrelated fields like CSS, Cloud Computing, Actuary, and Building Electrician, which seem irrelevant to the clinical research coordinator role and should be revised or removed for clarity.

Employment Type : Part-Time

Experience : years

Vacancy : 1

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