Senior CRA for Clinical Trials

2 days ago


Oslo, Oslo County, Norway IQVIA Argentina Full time

About the Position

IQVIA Argentina is seeking an experienced Senior CRA to join our site management team. As a key contributor, you will play a vital role in ensuring the successful execution of clinical trials.

Responsibilities

  • Monitor site performance against study protocols and regulatory requirements.
  • Partner with sites to identify opportunities for process improvements and optimized study execution.
  • Deliver comprehensive protocol and related study training to assigned sites, fostering strong relationships and open communication.
  • Investigate and resolve quality issues promptly, escalating concerns to relevant stakeholders as necessary.
  • Manage study timelines, coordinating regulatory submissions, subject recruitment, and data collection efforts.
  • Maintain accurate records of site documentation, ensuring Investigator's Site File (ISF) compliance with GCP and local regulations.
  • Document site management activities, findings, and actions taken through regular reports and correspondence.
  • Support project execution through collaboration with study teams.
  • Apply analytical and problem-solving skills to drive site financial management and invoice retrieval.

Requirements

  • Bachelor's Degree in a scientific discipline or healthcare, with preference given to candidates with clinical research experience.
  • A minimum of 3 years' experience in on-site monitoring, with a strong understanding of GCP and ICH guidelines.
  • Familiarity with Microsoft Office tools and proficiency in using laptop computers and mobile devices.
  • Excellent written and verbal communication skills, including fluency in English.
  • Proven ability to establish and maintain effective working relationships with colleagues, managers, and clients.


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