Test requisition - DO NOT APPLY
ICON · Milan, Italy
OtherFull-timeCompany career page
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Role summary
Site Management Associate I role supporting clinical trial operations at a global clinical research organization. The position involves assisting with site monitoring, protocol compliance, documentation, and cross-functional collaboration to maintain operational standards.
What they're looking for
- Bachelor's degree in life sciences, healthcare administration, or clinical research
- Strong organizational skills and attention to detail with multitasking ability
- Excellent communication and interpersonal skills for team collaboration
- Basic knowledge of clinical trial processes and regulatory requirements
- Willingness to travel approximately 25% as required
- Some clinical research, site management, or administrative experience preferred
What you'll be doing
- Assist in monitoring clinical trial sites for protocol adherence and GCP compliance
- Support site management activities including documentation, data entry, and performance tracking
- Collaborate with cross-functional teams to communicate and resolve site-related issues
- Maintain accurate records of site activities and prepare monitoring reports
- Participate in training initiatives to develop clinical trial management knowledge
Compensation€33,840.00-€42,300.00
Privacy & handoff
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