Clinical Research Associate

Há 11 horas


São Paulo, São Paulo, Brasil Icon Plc Tempo inteiro
Job Title: Clinical Research Associate

At ICON, we're driven by a shared vision to advance and improve patients' lives. As a Clinical Research Associate, you'll play a critical role in delivering excellence to our clients and patients at every touchpoint.

Overview:

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.

The Role:

  • Independent, proactive work to set up and monitor studies, complete reports and maintain documentation
  • Submitting protocol, consent documents for ethics/IRB approval, as well as preparing regulatory submissions
  • Balancing sponsor generated queries
  • Taking responsibility for study cost efficiency
  • Preparation and review of study documentation and feasibility studies for new proposals
  • Potential to assist in training and mentoring fellow CRAs

Requirements:

  • 18 months+ of monitoring experience in phase I-III trials as a CRA
  • College degree in medicine, science, or equivalent
  • Previous 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
  • Excellent written and verbal communication
  • Ability to work to tight deadlines
  • Availability to travel least 60% of the time (international and domestic -fly and drive) and should possess a valid driving license

Benefits:

We offer very competitive salary packages, regular benchmarking against competitors, and annual bonuses reflecting delivery of performance goals. We also provide a range of health-related benefits to employees and their families and offer competitive retirement plans.

At ICON, we're committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.



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