Clinical Research Coordinator

11 hours ago


Solna Municipality, Sweden IQVIA Argentina Full time
Job Overview

We are seeking a highly organized and detail-oriented individual to assist our clinical research team with the administration of clinical trials. This role will provide support for daily operations, including document management, data tracking, and communication with various stakeholders.

Key Responsibilities:
  1. Assist in the preparation, handling, and distribution of clinical trial documents and reports according to standard operating procedures.
  2. Provide administrative support to clinical research associates and regulatory teams, including updating and maintaining clinical systems and documentation.
  3. Track and manage case report forms, queries, and clinical data flow.
  4. Act as a central point of contact for project communications and correspondence.
  5. Aid in the preparation and maintenance of study files for completeness.
  6. Support the tracking and management of clinical trial supplies.
Qualifications:
  • Bachelor's degree or equivalent experience.
  • 3+ years of administrative support experience, preferably in a clinical research setting.
  • Excellent written and verbal communication skills.
  • Proficiency in Microsoft Office applications, particularly Word, Excel, and PowerPoint.
  • Ability to establish and maintain effective working relationships.
  • Familiarity with Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.


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