Site Contract Associate

🕒 July 15

🌐 Argentina, Brazil, +1 more countries – Remote

🇦🇷 Argentina – Remote 🇧🇷 Brazil – Remote 🇲🇽 Mexico – Remote

⏰ Full Time

🟢 Junior

🟡 Mid-level

✨ Associate

👻 Ghost score 23%

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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Parexel

WebsiteLinkedInAll Job Openings

10,000+ employees

Founded 1983

💼 Consulting

🏥 Healthcare

📦 Logistics

💰 Venture Round on 1990-01

Consulting • Healthcare • Logistics

Parexel is one of the world's largest clinical research organizations (CROs), providing comprehensive services for the clinical development process from Phase I to IV. The company specializes in portfolio management, clinical trial management, regulatory strategy, market access, and lifecycle management for biopharmaceuticals. Parexel aims to speed life-changing medicines to market by leveraging its clinical, regulatory, and therapeutic expertise. With a global team of over 21,000 professionals, Parexel works to integrate patient insights and innovative trial designs to develop treatments across therapeutic areas such as oncology, neuroscience, rare diseases, and more. It focuses on delivering patient-centric and efficient clinical trials.

📋 Description

• Responsible for negotiation with sites, finalization, and execution of all types of site contracts required for site activation including budget negotiations • Manage the negotiation, finalization, and execution of any amendments to the original contracts post site activation • Ensure the highest standard of quality of final documents and compliance with relevant regulatory requirements including ICH – GCP • Ensure that contracts meet needs of both clients and clinical trial sites, protecting best interests of clients and the company while nurturing positive relationships with clinical trial sites

🎯 Requirements

• 2 to 5 years of experience in clinical research site contracts support or related field • Experience negotiating, reviewing, and managing legal, commercial, or clinical trial-related agreements • Experience working with contract language, budgets, and financial terms • Strong analytical skills with the ability to interpret legal language and budget information • Excellent negotiation, organizational, interpersonal, and communication skills • Demonstrated ability to manage multiple projects and priorities in a fast-paced environment • Strong attention to detail and commitment to quality • Fluent written and spoken English • University degree in a related field; candidates with a degree in Law are highly relevant • Conversational Portuguese is a plus but not mandatory.

🏖️ Benefits

• N/A