Site Contract Specialist

PSI CRO; Çankaya; Hybrid; TRY 25,000 - 45,000; Full time

Job summary

Join a leading company in clinical research as a key support to clinical trials. You'll coordinate agreements and manage documentation in a dynamic environment while enhancing your skills and growing your career with the organization.

Qualifications

• Prior industry experience in clinical research.
• Full working proficiency in Turkish and English.
• Ability to plan, multitask, and work in a dynamic team environment.

Responsibilities

• Coordinate review and negotiation of clinical trial agreements.
• Perform administrative activities such as document collection and filing.
• Liaise with project teams on site contracting and grant negotiation.

Skills

Communication

Organizational skills

Attention to detail

Education

College/University degree

Job description

Company Description

We are the company that cares – for our staff, for our clients, for our partners, and for the quality of the work we do. A dynamic, global company founded in 1995, we bring together more than 3000 driven, dedicated, and passionate individuals. We work on the frontline of medical science, changing lives and bringing new medicines to those who need them.

Job Description

Join our international team and be a key support to clinical research projects as part of the start-up team. Work in a dynamic, multi-functional environment, gaining unique skills from various disciplines relevant to clinical research.

Office-based or remote in Türkiye

You will:

• Coordinate review and negotiation of clinical trial agreements and investigator grants between PSI staff and study sites.
• Perform administrative activities such as document collection/distribution, filing clinical trial agreements in the database, and maintaining 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.

Qualifications

• College/University degree or an equivalent combination of education, training, and experience.
• Prior industry experience in clinical research.
• Experience with legal documents related to clinical trial sites is a plus.
• Full working proficiency in Turkish and English.
• Strong communication and organizational skills.
• Attention to detail and ability to plan, multitask, and work in a dynamic team environment.

Additional Information

Take the next step in your clinical research career by coordinating a variety of tasks and enhancing your communication skills while growing with the company.