Site Contract Specialist

Summary

Join our international team and be a key support to clinical research projects. As part of the start-up team, you will work in a dynamic multi-functional environment, gaining unique skills from various disciplines relevant to clinical research. The position is office-based or remote in Türkiye. You will coordinate and negotiate clinical trial agreements and investigator grants, perform administrative activities, customize and prepare contractually binding site-specific documents, prepare executable contract versions, update and maintain tracking systems, and liaise with project teams. This role offers opportunities to grow your clinical research career and enhance communication skills.

Requirements

• College/University degree or an equivalent combination of education, training and experience
• Prior industry experience in clinical research
• Full working proficiency in Turkish and English
• Communication and organizational skills
• Attention to detail and ability to plan, multitask and work in a dynamic team environment

Responsibilities

• Coordinate review and negotiation of clinical trial agreements and investigator grants between PSI staff and study sites
• Perform administrative activities (documents collection/distribution, filing clinical trial agreements in the database and maintenance of local documentation)
• Customize and prepare contractually binding site-specific documents in cooperation with PSI Legal
• Prepare the executable version of the contract and coordinate the signature process
• Update and maintain relevant tracking and filing systems
• Liaise with project teams and other PSI departments on site contracting and grant negotiation matters

Preferred Qualifications

Prior experience with legal documents related to clinical trial sites is a plus