Site Contract Specialist I at PSI CRO

Sofia, Sofia-City, Bulgaria -

Full Time

Start Date

Immediate

Expiry Date

04 May, 26

Salary

0.0

Posted On

03 Feb, 26

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Contract Review, Budget Negotiation, Clinical Trial Agreements, Investigator Grants, Site-Specific Documents, CTMS Tracking, BPM Tracking, Contract Execution, Study Startup Support, Clinical Research, Legal Document Handling, MS Word, MS Excel, MS PowerPoint, Team Collaboration, Communication

Industry

Pharmaceutical Manufacturing

Description

Company Description PSI is a leading Contract Research Organization with more than 30 years in the industry offering a perfect balance between stability and innovation to both clients and employees. We focus on delivering quality and on-time services across a variety of therapeutic indications. Job Description Join our team to be the 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. Office-based during probation & Hybrid mode afterwards You will: Review and negotiate site budgets Facilitate the review and negotiation of clinical trial agreements (CTAs) and investigator grants between PSI Legal, the project team, and the study site Customize and prepare contractually binding site-specific documents in cooperation with PSI Legal Track CTA and investigator grant negotiation status in the Clinical Trial Management System (CTMS) and BPM Prepare the executable version of the contract, including grants, and coordinates the signature process Support the activities of Study Startup team Qualifications College/University degree or an equivalent combination of education, training & experience Previous experience working with study startup operations is required Experience with finance and negotiation is desirable Knowledge and experience with legal documents related to clinical trial sites would be considered a plus PC skills to be able to work with MS Word, Excel and PowerPoint Ability to plan and work in a dynamic team environment Communication and collaboration skills Native Bulgarian and proficiency in English Additional Information Advance your career in clinical research, coordinating a variety of tasks and learning new things while growing with the company.

Responsibilities

The specialist will review and negotiate site budgets and clinical trial agreements (CTAs) and investigator grants, acting as key support for clinical research projects during the start-up phase. Responsibilities also include customizing site-specific documents, tracking negotiation status in CTMS/BPM, and coordinating the final contract signature process.