
Senior Clinical Research Coordinator
Há 24 horas
A Clinical Research Associate at ICON works in a collaborative environment to ensure the successful execution of clinical studies. Key responsibilities include coordinating site initiation and monitoring visits, maintaining accurate study documentation, and submitting regulatory submissions as required. The ideal candidate possesses strong organizational and communication skills, with a proven track record in clinical research operations. If you're passionate about delivering high-quality results in a fast-paced environment, we encourage you to apply for this exciting opportunity.
Key Performance Indicators
- Coordination of site initiation and monitoring visits
- Maintenance of accurate study documentation
- Submission of regulatory submissions as required
- Collaboration with cross-functional teams to ensure timely completion of tasks
Requirements
- 2+ years of experience in clinical research operations, preferably in a CRO or pharmaceutical company
- Strong understanding of ICH GCP guidelines and ability to apply knowledge to real-world scenarios
- Excellent written and verbal communication skills, with proficiency in English and Portuguese
- Ability to work effectively in a pressurized environment with tight deadlines
What You'll Gain
This role offers a unique opportunity to develop your skills and expertise in clinical research operations. You'll work with a talented team to deliver high-quality results and contribute to the success of our clients' clinical studies. In addition to a competitive salary package, you'll have access to comprehensive health-related benefits and a range of retirement plans.
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