With our patients at the centre of all that we do, we help to accelerate the development of drugs and devices that save lives and improve quality of life.
Our people are our greatest strength, are at the core of our culture, and the driving force behind our success. ICON people have a mission to succeed and a passion that ensures what we do, we do well.
As a Clinical Research Associate at ICON, youll work within a large-scale, fast-paced environment within a global team to identify, select, initiate and close-out investigational sites for mainly late phase studies (IIIb/IV), ensuring adherence to applicable regulations and principles of ICH-GCP. We pride ourselves on our amazing company culture, where we work as one team to achieve industry-leading results.
The Role:
- Working independently and actively to coordinate activities to set up and monitor a study, completing accurate study status reports and maintaining study documentation
- Submission of protocol, consent documents for ethics/IRB approval and assist in preparing regulatory submissions as requested
- Balancing sponsor generated queries efficiently, manage and support sites and responsible for study cost-effectiveness
- Dependent on level of experience you may assist in training and mentoring less expert CRAs
- At least 12 months of independent, on-site monitoring experience
- Knowledge of ICG GCP guidelines and expertise to review and evaluate medical data
- Great command of the local language and) English (command of any other languages will be considered an advantage
- Ability to produce accurate work to tight deadlines within a pressurized environment
- You will be asked to travel around 60% of the time domestically (on rare occasions internationally) and should possess a valid driving license
Our success depends on the knowledge, capabilities and quality of our people. Thats why we are committed to developing our employees in a continuous learning culture one where we challenge you with engaging work and where every experience adds to your professional development.
At ICON, our focus is to provide you with a comprehensive and competitive total reward package that comprises, not only an excellent level of base pay, but also a wide range of variable pay and recognition programs. In addition, our best-in-class employee benefits, supportive policies and wellbeing initiatives are tailored to support you and your family at all stages of your career - both now, and into the future.
ICON, including subsidiaries, 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.
If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know through the form below.
