Clinical Research Associate

1 miesiąc temu


Warszawa, Mazovia, Polska IQVIA Pełny etat

Drive healthcare innovation by joining our team of skilled Clinical Research Associates at IQVIA.

Key Responsibilities

  1. Conduct site monitoring visits to ensure compliance with Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
  2. Collaborate with sites to adapt and track subject recruitment plans, enhancing predictability.
  3. Administer protocol training to assigned sites and establish regular communication to manage ongoing project expectations.
  4. Evaluate study site practices and escalate quality issues as necessary.
  5. Manage study progress by tracking regulatory submissions, recruitment, and data query resolution.
  6. Maintain accurate documentation of site management, monitoring visit findings, and action plans.

Requirements

  1. Life science degree education.
  2. Independent on-site monitoring experience.
  3. Experience handling multiple protocols and sites across various drug indications.
  4. Flexibility and ability to travel.
  5. Strong communication, written, and presentation skills.

IQVIA is a leading global provider of advanced analytics, technology solutions, and clinical research services to the life sciences industry. We aim to make a significant impact by driving innovation and pushing the boundaries of human science and data science to create a healthier world.



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