Site Management Associate I

About the role

Join PSI CRO’s international team as a Site Management Associate I, providing non‑monitoring site management and administrative support for clinical research projects in Turkey. This hybrid position is based in Ankara and involves coordinating between investigative sites, vendors, and project teams.

Key responsibilities

• Exchange data, documents and project‑relevant information between sites, vendors and the project team.
• Serve as the main site contact for administrative and non‑protocol matters, including regulatory submissions and site payments.
• Maintain Trial Master File (TMF) records, perform regular TMF checks and manage Investigator Site Files (ISF).
• Coordinate site audits, inspections and trial‑related training for investigators.
• Communicate with trial vendors, track supplies and ensure proper safety information flow.

Required profile

• College or university degree (relevant education, training and experience may be considered).
• Experience in Clinical Research or CRO environment, preferably international.
• Full working proficiency in English and Turkish.
• Strong organizational, planning and problem‑solving abilities.

Required skills

• Proficiency in standard MS Office applications.