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Clinical Research Coordinator

hace 2 meses

Lleida, Lérida, España IQVIA A tiempo completo
About the Role

We are seeking a highly skilled and detail-oriented Clinical Research Coordinator to join our team at IQVIA. As a pivotal member of our site team, you will be responsible for supporting clinical research studies and maintaining a safe study environment according to health and safety policies under the direction and delegation of the Principal Investigator.

Key Responsibilities
  1. Study Support: Provide administrative support to investigators and ensure the smooth running of clinical trials, including collecting patient data.
  2. Subject Safety: Safeguard the well-being of subjects, act as a volunteer advocate, and address subjects' concerns.
  3. Study Documentation: Maintain up-to-date study protocols, case report forms (CRFs), Electronic Data Capture (EDC) systems, and other study documents.
  4. Logistical Planning: Plan and coordinate logistical activity for study procedures according to the study protocol.
  5. Study Setup: 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.
  6. Data Management: Assist with data entry, data quality checking, and query resolution to ensure adherence to study protocol and quality control for content accuracy and completeness.
  7. Study Enrollment: Assist in study enrollment by recruiting, screening, and orienting volunteers according to the study protocol.
  8. Study Drug Management: Correct custody of study drug according to site standard operating procedures.
  9. Monitor Coordination: Coordinate with study monitor on study issues and effectively respond to monitor-initiated questions.
Requirements
  1. Education: BS/BA in life sciences or educational equivalent and/or relevant work experience in a clinical environment or medical setting.
  2. Knowledge: Basic knowledge of clinical trials, combined with in-depth knowledge of departmental, protocol, and study-specific operating procedures, consent forms, and study schedules.
  3. Medical Terminology: Basic knowledge of medical terminology.
  4. IT Competence: Strong IT competence, skilled in using MS Windows and Office applications such as Access, Outlook, Excel, and Word.
  5. Interpersonal Skills: Excellent interpersonal skills with the ability to establish and maintain effective working relationships with co-workers, managers, and clients.
  6. Organizational Skills: Good organizational skills with the ability to pay close attention to detail.