Site Contract Specialist at PSI CRO

Budapest, Central Hungary, Hungary -

Full Time

Start Date

Immediate

Expiry Date

22 Feb, 26

Salary

0.0

Posted On

24 Nov, 25

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Clinical Research, Contract Negotiation, Administrative Activities, Attention To Detail, Communication Skills, Organizational Skills, Multitasking, Team Environment, Legal Documents, Document Management, Database Maintenance, Project Coordination, Hungarian Language, English Language

Industry

Pharmaceutical Manufacturing

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 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 the key support to clinical research projects, as part of the start-up team, working in a dynamic multi-functional environment, gaining unique skills from various disciplines relevant to clinical research. This role is hybrid - Based in Budapest You will: 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. Qualifications College/University degree or an equivalent combination of education, training and experience Prior industry experience in clinical research Prior experience with legal documents related to clinical trial sites is a plus Full working proficiency in Hungarian and English 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, coordinating a variety of tasks and excelling your communication skills while growing with the company.

Responsibilities

The Site Contract Specialist will coordinate the review and negotiation of clinical trial agreements and investigator grants, while performing various administrative activities. This role involves customizing site-specific documents and liaising with project teams on contracting matters.