Site Contract Associate

Parexel

Site Contract Associate responsible for negotiation and execution of site contracts for clinical trials at Parexel. Contributing to a global clinical research team working remotely from Argentina, Mexico, or Brazil.

Posted 7/15/2026full-timeRemote • 🇦🇷 ArgentinaJuniorMid-LevelWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in negotiating and managing clinical research site contracts, ensuring compliance with regulatory requirements and maintaining high-quality standards. Strong analytical and communication skills facilitate effective relationship management with clients and clinical trial sites.

Highest-signal resume keywords

Clinical Research Site Contracts ManagementNegotiation of Legal AgreementsBudget Management and Financial TermsRegulatory Compliance (ICH – GCP)Analytical Skills in Legal Language Interpretation

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Contract NegotiationBudget NegotiationContract Language ReviewClinical Trial AgreementsQuality AssuranceRegulatory ComplianceProject ManagementAttention to DetailAnalytical SkillsInterpersonal Skills

Soft Skills

Excellent Communication SkillsOrganizational SkillsNegotiation Skills

Industry Keywords

Clinical ResearchSite ActivationLegal AgreementsCommercial AgreementsClinical Trial SitesFast-Paced EnvironmentUniversity Degree in Related FieldDegree in LawFluent EnglishConversational Portuguese

Tech Stack

Tools & technologies

Google Cloud Platform

About the role

Key responsibilities & impact

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

What you’ll need

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

Comp & perks

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