Senior Clinical Research Associate

hace 3 días


Palma, Baleares, España Pharmiweb A tiempo completo
Job Title: Senior Clinical Research Associate

We are seeking a highly skilled and experienced Senior Clinical Research Associate to join our team in Madrid, Spain. As a Senior CRA, you will be responsible for coordinating activities to set up and monitor clinical studies, ensuring adherence to applicable regulations and principles of ICH-GCP.

Key Responsibilities:
  • Working independently to coordinate study activities, including setting up and monitoring investigational sites
  • Completing accurate study status reports and maintaining study documentation
  • Submitting protocol, consent documents for ethics/IRB approval and assisting in preparing regulatory submissions as requested
  • Participating in preparing and reviewing study documentation and feasibility studies for new proposals as required
  • Balancing sponsor generated queries efficiently and responsible for study cost-effectiveness
  • Assisting in training and mentoring less expert CRA's and/or lead CRA's working on international projects
Requirements:
  • 2-3 years+ of monitoring experience in phase I-III trials as a CRA
  • Knowledge of ICG GCP guidelines and expertise to review and evaluate medical data
  • Excellent written and verbal communication in English
  • Ability to produce accurate work to tight deadlines within a pressurized environment
  • Valid driving license and willingness to travel at least 60% of the time (international and domestic)
What We Offer:

Our success depends on the quality of our people. That's why we've made it a priority to build a diverse culture that rewards high performance and nurtures talent. In addition to your competitive salary, ICON offers a range of additional benefits, including various annual leave entitlements, health insurance offerings, competitive retirement planning, and a global Employee Assistance Programme.

We are an equal opportunity and inclusive employer, committed to providing a workplace free of discrimination and harassment. If you need a reasonable accommodation for any part of the application process, please let us know or submit a request here.

Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless - there's every chance you're exactly what we're looking for here at ICON.



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