Senior Clinical Research Associate
hace 2 semanas
As a key member of our team at ICON, you will be responsible for managing clinical trials and ensuring the highest level of quality and accuracy in our research.
With a strong background in biopharmaceutical clinical research, you will be partnering with pharmaceutical companies to discover and develop life-changing treatments.
Key Responsibilities:
- Maintain accurate and complete data in our systems.
- Participate in training and mentoring new staff.
- Conduct and manage projects, including implementing study plans and coordinating with investigators.
- Identify potential problems and improve timelines.
- Coordinate and advise on all necessary activities for setting up and monitoring studies, including:
- Identifying investigators.
- Ensuring timely submission of protocol documents.
- Conducting regular monitoring visits.
- Completing accurate study status reports.
- Dealing with sponsor queries.
- Ensuring satisfactory close-out of investigator sites.
- Participating in the preparation and review of study documentation.
- Ensuring correct archiving of files.
Requirements:
- Bachelor's degree in a health, life sciences, or relevant field.
- Minimum 8 years of biopharmaceutical clinical research experience.
- Availability to travel.
- Fluent English and host country language skills.
What ICON Offers:
We value diversity, inclusion, and belonging at ICON. Our team is dedicated to providing an inclusive and accessible environment for all candidates. We offer a competitive salary and a range of benefits designed to support your well-being and work-life balance.
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