Clinical Research Coordinator - Cádiz, España - IQVIA Argentina

Are you currently searching for an opportunity in the field of Clinical Research? Do you aspire to be part of a top-tier company? If you do, we welcome you to join our team at IQVIA, where we are currently seeking a Clinical Research Coordinator.

This part-time position (24 hours per week) is designed for an 11-month duration and aims to provide support to the site in Cadiz as they conduct a clinical trial in the specialized area of Cardiology .

As a core team member of the site, you will be tasked with a range of administrative duties to assist investigators, ensure the seamless progress of clinical trials, and aid in the collection of patient data.

Responsibilities on a daily basis will involve:

• Contributing to clinical research studies and upholding a secure study environment in compliance with health and safety protocols under the guidance of the Principal Investigator
• Ensuring the welfare of subjects, serving as a volunteer advocate, and addressing any concerns raised by the subjects
• Keeping all study protocols, case report forms (CRFs), Electronic Data Capture (EDC) systems, and other study-related documents current
• Planning and organizing logistical activities for study procedures as per the study protocol
• Executing clinical setup and readiness for the study, including labeling specimen collection tubes and containers, managing the inventory of necessary supplies, and setting up or troubleshooting equipment as required
• Assisting in data entry, conducting quality checks on data, and resolving queries to maintain compliance with the study protocol and ensuring content accuracy and completeness
• Facilitating study enrollment by recruiting, screening, and orienting volunteers in line with the study protocol
• Ensuring proper handling of study drugs following site standard operating procedures
• Collaborating with study monitors on study-related matters and providing prompt and effective responses to queries initiated by the monitor

We are seeking candidates with the following qualifications and expertise:

• A degree in life sciences or equivalent education, or relevant work experience in a clinical environment or medical setting, e.g., clinical research coordination, nursing, medical assistance, or other medical professions
• Fundamental understanding of clinical trials, coupled with detailed knowledge of departmental, protocol, and study-specific operational procedures, consent forms, and study timelines
• Basic familiarity with medical terminology
• Proficiency in IT, adept at using MS Windows and Office applications like Access, Outlook, Excel, and Word
• Exceptional interpersonal talents enabling the establishment and maintenance of productive relationships with colleagues, supervisors, and clients
• Strong organizational abilities with a keen eye for detail

IQVIA stands as a premier global entity offering cutting-edge analytics, technological solutions, and clinical research services to the life sciences industry. Our commitment lies in expanding the frontiers of human and data sciences to generate the most significant impact possible - assisting our clientele in shaping a healthier world. Find out more at