About this role
About the Role The Site Management Associate I supports site management activities for PSI CRO's clinical trials, ensuring coordination between sites, study teams, and sponsors to maintain compliant and efficient trial operations. What You'll Do
- Assist with site management activities for assigned sites to ensure smooth trial conduct
- Coordinate documentation, regulatory submissions, and day-to-day site communications
- Monitor study timelines, assist with site initiation visits, and maintain trial-master-file quality
- Liaise with investigators, clinical staff, and data management teams to support trial needs What We're Looking For
- Bachelor's degree in life sciences or related field
- Strong organizational and communication skills with attention to detail
- Ability to work cross-functionally in a fast-paced clinical research environment
- Familiarity with GCP/ICH guidelines and clinical trial processes Nice to Have
- Experience in site management or clinical operations
- Familiarity with electronic trial master file systems and CTMS