Site Management Associate
hace 1 mes
Site Management Associate
At ICON, we are proud to foster an inclusive environment driving innovation and excellence. As a Site Management Associate, you will be responsible for managing, implementing, and monitoring clinical studies within a global organization.
The work of a Site Management Associate is varied and challenging, offering you the opportunity to use your language skills. Your responsibilities will include:
- Identifying, training, and closing out study sites
- Conducting remote site monitoring visits and/or targeted on-site visits as needed
- Training site staff on essential processes and systems
- Collection and management of essential documents
- Managing study sites and protocols, ensuring accurate data reporting and timely completion
- Serving as the primary point of contact for investigator site staff
- Performing study tracking
What You Need
To be successful in this role, you will possess a clinical or life science degree and the ability to adapt quickly to new computer systems. At least two years of previous site management and/or monitoring experience, ideally as a CRA or In-house CRA, is required. Experience working within a CRO, Pharmaceutical, or hospital/healthcare environment is also necessary. A great command of French and English is required; additional languages are a plus.
What ICON Can Offer You
Our success depends on the quality of our people. We offer a competitive salary, various annual leave entitlements, health insurance offerings, and competitive retirement planning. We focus on well-being and work-life balance opportunities for you and your family.
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