Clinical Research Associate II

3 settimane fa


Palermo, Sicilia, Italia Pharmiweb A tempo pieno
Study Start Up Associate II

At ICON, we're proud to foster an inclusive environment driving innovation and excellence. As a Study Start Up Associate II, you'll play a crucial role in ensuring physicians at our research sites are prepared to start clinical trials of investigational products.

The Role

Review and negotiate clinical site investigator contracts and budgets.

Stay connected with investigative sites, sponsors, and internal personnel regarding contract status and related documents.

Prepare and coordinate contractual documents and correspondence.

Facilitate the indemnification process between the study sponsor and the site.

Function as an internal consultant on study budgets, including investigator payments, training documentation, and group training.

What You Need

A bachelor's degree in Paralegal Studies, Juris Doctor (law) degree, or related experience is preferred.

At least 3 years of experience with submissions and CTR Regulations.

Experience in a clinical research environment.

Italian Speaker.

Benefits of Working at ICON

We offer competitive salary packages, annual bonuses, and a range of health-related benefits to employees and their families. Our inclusive environment rewards high performance and nurtures talent, making us a great place to work and grow.

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