Responsibilities

  • As a Clinical Research Associate you'll work within a large-scale, fast-paced environment alongside a close-knit team of highly qualified CRAs to identify, select, initiate and close-out investigational sites for clinical studies in phases II - IV, ensuring adherence to applicable regulations and principles of ICH-GCP. 
  • You will do independent, proactive work to set up and monitor studies, complete reports and maintain documentation, and submit protocol, consent documents for ethics/IRB approval, as well as prepare regulatory submissions.
  • You'll be managing sponsor generated queries, and taking responsibility for study cost effectiveness.
  • Preparation and review of study documentation and feasibility studies for new proposals.
  • You will have the potential to assist in training and mentoring fellow CRAs.
REQUIRED
  • A University degree in medicine, science, or equivalent.
  • You must have significant previous independent monitoring experience in medium sized studies, including study start-up and close-out.
  • Knowledge of ICH-GCP guidelines and ability to review and evaluate medical data.
  • You have excellent written and verbal communication and the ability to work to tight deadlines.
  • Availability to travel at least 60% of the time