A college/university degree or an equivalent combination of education, training, and experience.Previous industry experience in clinical research is required.Experience with legal documents related to clinical trial sites is a plus.Full working proficiency in Hungarian and English.Strong communication and organizational skills.Exceptional attention to detail, with the ability to plan, multitask, and thrive in a dynamic team environment.
About the job
Become an integral part of our international team as a Site Contract Specialist, supporting clinical research projects within a dynamic start-up environment. This hybrid role, based in Budapest, offers a unique opportunity to acquire diverse skills from various fields relevant to clinical research.
Your responsibilities will include:
Coordinating the review and negotiation of clinical trial agreements and investigator grants between PSI staff and study sites.
Conducting administrative tasks such as collecting and distributing documents, filing clinical trial agreements in the database, and maintaining local documentation.
Customizing and preparing site-specific contract documents in collaboration with PSI Legal.
Preparing the final executable version of contracts and managing the signature process.
Updating and maintaining relevant tracking and filing systems.
Collaborating with project teams and other PSI departments on site contracting and grant negotiation issues.
About psicro
At psicro, we prioritize the well-being of our staff, clients, and partners, alongside the quality of our work. Founded in 1995, we are a dynamic global company bringing together 3,000 dedicated and passionate individuals. Our mission is to work at the forefront of medical science, making a difference in lives by delivering new medicines to those in need.
This job posting is no longer active and is not accepting applications.
A college/university degree or an equivalent combination of education, training, and experience.Previous industry experience in clinical research is required.Experience with legal documents related to clinical trial sites is a plus.Full working proficiency in Hungarian and English.Strong communication and organizational skills.Exceptional attention to detail, with the ability to plan, multitask, and thrive in a dynamic team environment.
About the job
Become an integral part of our international team as a Site Contract Specialist, supporting clinical research projects within a dynamic start-up environment. This hybrid role, based in Budapest, offers a unique opportunity to acquire diverse skills from various fields relevant to clinical research.
Your responsibilities will include:
Coordinating the review and negotiation of clinical trial agreements and investigator grants between PSI staff and study sites.
Conducting administrative tasks such as collecting and distributing documents, filing clinical trial agreements in the database, and maintaining local documentation.
Customizing and preparing site-specific contract documents in collaboration with PSI Legal.
Preparing the final executable version of contracts and managing the signature process.
Updating and maintaining relevant tracking and filing systems.
Collaborating with project teams and other PSI departments on site contracting and grant negotiation issues.
About psicro
At psicro, we prioritize the well-being of our staff, clients, and partners, alongside the quality of our work. Founded in 1995, we are a dynamic global company bringing together 3,000 dedicated and passionate individuals. Our mission is to work at the forefront of medical science, making a difference in lives by delivering new medicines to those in need.