Clinical Research Coordinator - Valencia, Spain
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, 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.
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