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At ICON, we're a world-leading healthcare intelligence and clinical research organization that's dedicated to fostering an inclusive environment where innovation and excellence thrive. As a Clinical Research Associate at ICON, you'll be part of a close-knit team of highly qualified CRAs working on large-scale, fast-paced projects.
Company OverviewWe're proud to have a company culture that works as one team to achieve industry-leading results. Our success depends on the quality of our people, which is why we've made it a priority to build a diverse culture that rewards high performance and nurtures talent.
Job Description- You'll work independently to coordinate activities, set up and monitor studies, complete accurate study status reports, and maintain study documentation.
- Submission of protocol, consent documents for ethics/IRB approval, and assisting 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.
- Dependent on level of experience, you may assist in training and mentoring less expert CRAs and/or lead CRAs working on international projects.
- 18 months+ of independent monitoring experience in phase I-III trials as a CRA, working for a CRO or pharma company.
- Knowledge of ICH GCP guidelines and expertise to review and evaluate medical data.
- Excellent written and verbal communication skills in English.
- Able to produce accurate work to tight deadlines within a pressurized environment.
- Possess a valid driving license for traveling within Portugal.
We offer very competitive salary packages and regularly benchmark them against our competitors. Our annual bonuses reflect delivery of performance goals – both ours and yours. We provide a range of health-related benefits to employees and their families, including competitive retirement plans, life assurance, and more.