Senior Clinical Research Associate

1 month ago


Blue Bell, Pennsylvania, United States ICON plc Full time
Job Summary

We are seeking a highly skilled Senior Clinical Research Associate to join our team at ICON plc. As a Senior CRA, you will play a critical role in the success of our clinical trials, working closely with our team to identify, select, initiate, and close-out investigational sites.

Key Responsibilities:

  • Coordinate activities to set up and monitor studies, ensuring accurate study status reports and maintaining study documentation.
  • Submit protocol and consent documents for ethics/IRB approval and assist in preparing regulatory submissions as requested.
  • Participate in preparing and reviewing study documentation and feasibility studies for new proposals.
  • Balancing sponsor-generated queries efficiently and responsible for study cost-effectiveness.
  • Assist in training and mentoring less-experienced CRAs and/or lead CRAs working on international projects.

Requirements:

  • 18 months+ of monitoring experience in phase I-III trials as a CRA.
  • Knowledge of ICH 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:

  • Competitive salary and benefits package.
  • Opportunities for career growth and professional development.
  • Collaborative and inclusive work environment.
  • Recognition and rewards for high performance.

At ICON plc, we are committed to providing a workplace free of discrimination and harassment. We welcome applications from diverse candidates and are an equal opportunity employer.



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