Clinical Research Associate II

hace 4 semanas


Madrid, Madrid, España Pharmiweb A tiempo completo

Key Responsibilities:

As a Clinical Research Associate II, you will be responsible for performing all study start-up activities for a clinical trial. This includes participating in Pre SIV activities and managing and driving the strategy for the Pre SIV / start-up tasks of the study.

You will also be responsible for generating visit/contact reports, using judgment to identify site issues and problem-solving to direct resolution. Additionally, you will develop strategies to configure, distribute, and collect, and review and approve, high-quality country-specific and/or site-specific documents or essential regulatory documents (SRP) and any updated or amended regulatory documentation.

Requirements:

  • Previous experience in study set-up / site initiation / study start-up experience or equivalent experience in a clinical research environment
  • Understanding of clinical trials methodology and terminology, including experience with EU CTR
  • Good previous Clinical Site Agreement (CSA) and site contracts experience is desirable
  • Fluent command of Spanish and English languages

What We Offer:

At Pharmiweb, we offer a dynamic and challenging work environment that allows our employees to grow and develop their skills. We are committed to providing our employees with the necessary tools and resources to succeed in their roles.



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