Site Contract Specialist I

🔥 2 hours ago

🇺🇸 United States – Remote

⏰ Full Time

🟢 Junior

🟡 Mid-level

👻 Ghost score 10%

What it means: how likely this posting is sitting open without active hiring.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.How we score it: age, reposts, open roles vs team size, how fast jobs close, and whether pay is listed.Fine print: an estimate from public data, not a judgment of the company. Real jobs can score high, so treat it as a hint, not a fact.

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PSI CRO AG

WebsiteLinkedInAll Job Openings

1001 - 5000 employees

Founded 1996

🏥 Healthcare

💼 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

• Facilitate negotiations of site agreements and budgets to align with the site activation plan • Customize and prepare country- and site-specific agreements and organize translations • Track the status of site agreement and budget negotiations • Prepare executable versions of site agreements and budgets • Coordinate the signature process • File executed site agreements in the Trial Master File • Update all concerned functions on the site contracting process

🎯 Requirements

• College or university degree, or an equivalent combination of education, training, and experience • Equivalency requires a minimum of 2 years’ experience in a relevant environment • Minimum 2 years’ experience in the clinical research industry • Previous experience negotiating site budgets • Knowledge of and experience with legal documents related to clinical trial sites and medical terminology is a plus • Must not require a work visa for employment or continued employment now or anytime in the future • Ability to work anywhere in the United States

🏖️ Benefits

• Remote work arrangement • Opportunity to work with a dynamic, global company • Work contributing to medical science and bringing new medicines to patients • People-focused company culture