Evestia Clinical

Conduct routine and for-cause audits including site, vendor, and internal process audits to ensure compliance with regulations and SOPs. Collaborate with project teams to develop resolution plans and CAPAs while serving as a regulatory reference for sponsors.

The CRA is responsible for protecting the rights and safety of clinical trial participants while ensuring data accuracy and verifiability. Key duties include performing site visits, ensuring protocol compliance, and liaising between sponsors and investigators.

The CRA is responsible for protecting the rights and safety of clinical trial participants while ensuring data accuracy and completeness. Key duties include performing all types of site visits and ensuring compliance with protocols, ICH/GCP, and company SOPs.

The role involves performing all types of site visits to ensure clinical trial participants' safety and data accuracy. Responsibilities include maintaining regulatory compliance and liaising between sponsors, investigators, and project teams.