Clinical Research Coordinator Valencia

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 are looking for a Clinical Research Coordinator.

This full time role is planned for approx. 6 months and is to support the site in Valencia in conducting a clinical trial in the field of Cardiovascular.

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 client
• Good organizational skills with the ability to pay close attention to detail.

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IQVIA is a leading global provider of clinical research services commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at .

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements misrepresentations or material omissions during the recruitment process will result in immediate disqualification of your application or termination of employment if discovered later in accordance with applicable law. We appreciate your honesty and professionalism.

At IQVIA we believe that diversity inclusion and belonging empower our mission to accelerate innovation for a healthier world. We create a culture of belonging by valuing the perspectives of all talented employees worldwide and providing them with the opportunity to power smarter healthcare for everyone everywhere. When our talented employees bring their authentic selves and their diverse experiences to work they enable us to accomplish extraordinary things. Multifaceted thought processes spark innovation. Multi-talented collaboration harnesses innovation to deliver superior outcomes.