Site Contract Specialist I

đŸ”„ 16 hours ago

đŸ‡ČđŸ‡œ Mexico – Remote

⏰ Full Time

🟡 Mid-level

🟠 Senior

✹ Contract Specialist

đŸ‘» Ghost score 10%

infoinfo

đŸ—ŁïžđŸ‡Ș🇾 Spanish Required

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Logo of PSI CRO AG

PSI CRO AG

1001 - 5000 employees

Founded 1996

đŸ„ Healthcare

đŸ’Œ Consulting

📩 Logistics

Healthcare ‱ Consulting ‱ Logistics

PSI CRO AG is a global contract research organization (CRO) that specializes in conducting clinical trials. The company focuses on delivering pivotal Phase 2 and 3 clinical trials across various therapeutic areas, including Inflammatory Bowel Diseases, Oncology, Hematology, Infectious Diseases, Multiple Sclerosis, and Rare Diseases. PSI utilizes a proprietary technology platform for clinical trial planning and financial tracking to ensure trials are conducted on time and within budget. The company is recognized for its expertise, quality, compatibility, and reliability, having been awarded the CRO Leadership Awards for multiple consecutive years.

📋 Description

‱ 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) ‱ Prepare the executable version of the contract, including grants, and coordinate the signature process ‱ File executed contracts in the Trial Master File and maintain local documentation ‱ Liaise with the project team, translation, and legal departments on site contracting and grant negotiation matters ‱ Support the activities of the Study Startup team if needed

🎯 Requirements

‱ College/University degree or an equivalent combination of education, training & experience ‱ Fluency in Spanish and English, oral and written ‱ 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 ‱ Only CVs in English will be considered

đŸ–ïž Benefits

‱ Remote work / home-based position in Mexico

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