Senior Site Manager

About the role

The Senior Site Manager (Site Manager II) acts as the primary liaison between Johnson & Johnson and investigational sites in Beijing, overseeing all phases of clinical trials from start‑up to close‑out. The role ensures compliance with protocol, SOPs, GCP and local regulations while supporting subject recruitment, monitoring and data integrity.

Key responsibilities

• Serve as the main local contact for assigned trial sites, handling feasibility, initiation, monitoring (including remote) and close‑out activities.
• Implement risk‑based monitoring, ensure timely issue resolution, and maintain accurate training records for site staff.
• Manage site supplies, clinical drug handling, adverse event reporting, and data entry timelines.
• Collaborate with Local Trial Manager, Clinical Trial Assistant and Central Study Team to accelerate site activation and maintain study progress.
• Document all monitoring activities, prepare visit reports, and support quality audits and corrective actions.

Required profile

• Bachelor’s degree in Life Sciences, Nursing or related scientific field (or equivalent experience).
• Minimum of 2 years of clinical trial monitoring experience, with knowledge of therapeutic area preferred.
• Strong understanding of GCP, company SOPs, local regulations and protocol‑specific procedures.
• Excellent written and oral communication in English and the local language.

Required skills

• Good Clinical Practice (GCP) compliance.
• Clinical trial monitoring and site management.
• Proficiency with trial management software and IT tools.