Clinical Research Coordinator Specialist

hace 4 días

Málaga, Málaga, España Iqvia Argentina A tiempo completo
Role Overview

We are seeking a highly motivated Clinical Research Coordinator to join our team in Malaga. 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.

About the Role

This part-time (24 hours per week) role is to support the site in Malaga. The successful candidate will have excellent organizational skills with the ability to pay close attention to detail.

Responsibilities
  • 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.
Requirements
  • Bachelor's degree in Life Sciences or equivalent experience in a clinical environment or medical setting.
  • 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.
  • Estimated Salary: $40,000 - $55,000 per year.

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