Clinical Research Associate II
4 settimane fa
At ICON, we are committed to fostering an inclusive environment that drives innovation and excellence. We are seeking a highly skilled Clinical Research Associate II to join our team.
The successful candidate will be responsible for monitoring and managing clinical sites, ensuring compliance with regulatory requirements and study protocols. Key responsibilities include:
- Developing strong site relationships through regular communication and site visits
- Applying SOPs, Clinical Monitoring Plans, and study protocols to ensure site compliance
- Identifying and qualifying potential investigators
- Performing pre-study site visits and site initiation visits
- Monitoring site compliance with study protocol and GCP
- Providing initial and ongoing training to clinical investigators and site staff
The ideal candidate will have a strong background in clinical research, excellent communication and interpersonal skills, and the ability to work independently with minimal supervision. If you are a motivated and detail-oriented individual who is passionate about clinical research, we encourage you to apply.
What We Offer:
- A competitive salary and benefits package
- Opportunities for professional growth and development
- A dynamic and inclusive work environment
We are an equal opportunities employer and welcome applications from diverse candidates. If you require any accommodations during the application process, please let us know.
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