Job Title

Lead clinical operations as a Site Activation Partner I focusing on compliance and timely site activations. Partner with teams to ensure high-quality Investigator Initiation Packages and effective issue resolution. The Site Activation Partner I is essential for managing operational activities from start-up through to study close-out. This position requires collaboration with regulatory groups and coordination of necessary documentation to secure site initiation approvals. Candidates should bring at least two years of experience in clinical trials and a solid understanding of ICH/GCP standards. Key Responsibilities: Initiate and manage Investigator Initiation Packages for site approval Coordinate with teams to resolve site activation issues Maintain compliance tracking within clinical trial systems Collaborate on regulatory and ethical document submissions Address and resolve investigator site concerns promptly Requirements: High school diploma with suitable education and experience Minimum 2 years in clinical trials or site activation Familiarity with FDA and global regulations Knowledge of clinical trial methodologies Fluency in English and local language Bring your operational expertise and commitment to quality in clinical trials to this impactful role. #J-18808-Ljbffr