Clinical Research Associate
hace 1 semana
ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to be part of our mission to shape the future of clinical development.
Key Responsibilities:- Work independently and actively to 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.
- Balance 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.
- 2-3 years+ of monitoring experience in phase I-III trials as a CRA.
- Knowledge of ICG GCP guidelines and expertise to review and evaluate medical data.
- Excellent written and verbal communication in English.
- Ability to produce accurate work to tight deadlines within a pressurized environment.
- Remote work with occasional travel, requiring a valid driving license.
Our success depends on the quality of our people. That's why we've made it a priority to build a diverse culture that rewards high performance and nurtures talent.
In addition to your competitive salary, ICON offers a range of benefits, including annual leave entitlements, health insurance, retirement planning, and more.
We're an equal opportunity and inclusive employer, committed to providing a workplace free of discrimination and harassment.
If you're interested in this role, but unsure if you meet all the requirements, we encourage you to apply - there's every chance you're exactly what we're looking for here at ICON.
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