Senior Clinical Research Associate
4 weeks ago
As a Senior Clinical Research Associate, you will be responsible for working on multiple trials within Oncology, focusing on quality of life and regional travel. You will demonstrate leadership skills through involvement in specific initiatives and mentor junior team members. Your responsibilities will include acting as a lead site manager, training other site managers, and developing site start-up documents. You will also provide a "site manager's voice" when reviewing study documents and represent LTMs or SMs on SMTs/meetings. Additionally, you will take over LTM role reports review for sites assigned to other SMs from the same trial and support country budget development and/or contract negotiation. Your primary interfaces will be with the Provider Functional Manager, Clinical Trial Assistant, Local Trial Manager, and Central Study Team.
Requirements:
- Regional location in Miami, FL
- Bachelor's degree in Biological Sciences or equivalent
- Minimum 3 years' experience in monitoring pharmaceutical industry clinical trials
- Minimum 1-3 years' experience monitoring Oncology trials
- Bilingual in Spanish
- Analytical/risk-based monitoring experience is an asset
- Ability to actively drive patient recruitment strategies at assigned sites
- Ability to partner closely with investigator and site staff to meet all of our study timelines
- Ability to operate and use various systems and databases
- Strong communication and influencing skills
- Knowledge of Good Clinical Practice, ICH guidelines, and local regulatory requirements
What ICON Can Offer:
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 various annual leave entitlements, health insurance, retirement planning, and a global employee assistance program.
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