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Clinical Research Associate Opportunity
2 semanas atrás
Clinical Research Associate Role Overview
We are seeking a skilled Clinical Research Associate to join our dynamic team. As a key member of our research department, you will be responsible for overseeing and coordinating clinical trials, ensuring compliance with regulations, and collecting and analyzing critical data.
Key Responsibilities:
- Coordinate all activities for setting up and monitoring a study, completing accurate study status reports, and maintaining study documentation.
- Run sponsor-generated queries efficiently and take responsibility for study cost efficiency.
- Develop and maintain strong relationships with stakeholders, clinical investigators, and site staff.
- Ensure patient safety by adhering to ICON's procedures, protocols, and regulatory requirements.
Requirements:
- Minimum 2 years of experience in a similar role.
- Deep understanding of ICH GCP Compliance.
- Excellent English language skills - writing, reading, communication.
- Highly motivated individual with attention to detail.
- Complete Bachelor's degree in life science or related discipline.
- Ability to travel extensively (at least 60%) and possess a valid driver's license.
Benefits:
Our success relies on the quality of our people. We offer competitive salary packages, regular benchmarking against industry standards, and performance-based bonuses. Additionally, we provide a range of health-related benefits, including comprehensive health insurance and retirement plans. Our culture is driven by four core values: Accountability & Delivery, Collaboration, Partnership, and Integrity.
Diversity, Inclusion & Belonging:
At our organization, diversity, inclusion, and belonging are fundamental to our culture and values. Our rich diversity makes us more innovative, enabling us to better serve our people, patients, customers, and communities. We strive to create an inclusive and accessible environment for all candidates.
