Medical Monitor Professional

4 days ago


Copenhagen, Copenhagen, Denmark IQVIA Argentina Full time

The Role

IQVIA Argentina is seeking a Medical Monitor Professional to join our team. The ideal candidate will have experience in clinical research and be able to monitor clinical studies effectively.

Key Responsibilities

  1. Monitor clinical sites to ensure compliance with Good Clinical Practice (GCP).
  2. Collaborate with sites to develop and track subject recruitment plans to enhance predictability.
  3. Provide protocol and related study training to assigned sites and maintain regular communication.
  4. Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations.
  5. Monitor study progress by tracking regulatory submissions, case report form completion, data query generation, and resolution.
  6. Maintain accurate records of site management, monitoring visit findings, and action plans.
  7. Collaborate with study team members for project execution support as needed.

Requirements

  • Bachelor's degree in a scientific discipline or healthcare preferred.
  • At least 2 years of on-site monitoring experience.
  • Excellent knowledge of clinical research regulatory requirements, GCP, and ICH guidelines.
  • Strong analytical and problem-solving skills.
  • Excellent communication and interpersonal skills.


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