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Senior Clinical Research Associate

2 meses atrás

São Paulo, São Paulo, Brasil Icon Plc Tempo inteiro
About the Role

As a Senior Clinical Research Associate at ICON, you will play a key role in the success of our clinical trials. Your primary responsibility will be to work independently and collaboratively with a close-knit team of highly qualified CRAs to identify, select, initiate, and close-out investigational sites for clinical studies in phases II - IV.

Key Responsibilities:

  • Coordinate activities to set up and monitor a study, completing accurate study status reports and maintaining study documentation
  • Submit protocol, 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 as required
  • Balancing sponsor generated queries efficiently and responsible for study cost-effectiveness
  • Dependent on level of experience, assist in training and mentoring less expert CRA's and/or lead CRA's working on international projects

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
  • Advanced English to read, write and Speak
  • Need to have vaccine/oncology experience

What We Offer:

  • Very competitive salary packages
  • Annual bonuses reflecting delivery of performance goals
  • A range of health-related benefits to employees and their families
  • Competitive retirement plans and related benefits such as life assurance

About ICON:

ICON is an equal opportunity and inclusive employer and is 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.