Site Activation Partner I

The Site Activation Partner I role at Parexel focuses on managing and coordinating clinical trial site activation activities, ensuring timely regulatory approvals, and maintaining essential documentation throughout the study lifecycle. This position involves collaborating with investigators, ethics committees, and internal teams to resolve site issues, support audits, and ensure compliance with Good Clinical Practices and company standards. The role requires strong organizational skills, attention to detail, and proficiency in clinical trial management systems to drive operational efficiency and study success.