Site Management Associate

About the role

Syneos Health is a leading fully‑integrated life sciences services organization that partners with innovators across drug development and commercialization. The Clinical Solutions team applies a drug‑development mindset and deep expertise to understand customer needs and shape solutions. As a Site Management Associate, you will perform site‑management activities in compliance with SOPs, support site identification, qualification, start‑up, monitoring, and close‑out, maintain documentation, ensure regulatory compliance, and collaborate with sponsors and site staff to advance clinical trials.

Responsibilities

• Perform site management activities in compliance with the Company and Sponsor (if applicable) Standard Operating Procedures (SOPs) and Work Instructions (WIs).
• Assure compliance with local regulations and appropriate guidance depending on assigned study design / classification; may include Good Pharmacoepidemiology Practices (GPP) and/or International Conference on Harmonization - Good Clinical Practice (ICH‑GCP).
• Conduct site management activities as per agreed Scope of Work (SoW), Site Management Plan (SMP) and relevant guidelines.
• Site identification – may contact sites to obtain interest in study participation, confirm contact details, retrieve documents for consideration, etc.
• Site Qualification – Ensures selection of appropriate sites for assigned studies.
• Site Start‑Up – With minimal supervision, ability to perform activities for assigned sites working with study start‑up and regulatory.
• Conduct of all remote and on‑site monitoring activities through all study stages.
• Routinely reviews the Investigator Site File (ISF) for accuracy, timeliness and completeness; reconciles contents of the ISF with the Trial Master File (TMF); ensures the investigator/physician site is