Site Contracts Associate II

Responsibilities

• Draft, review, and negotiate clinical study agreements, service agreements, and related legal documents.
• Ensure all final documents comply with applicable laws, regulations, and ICH-GCP guidelines.
• Act as a key communication liaison between site contracts staff and internal/external customers.
• Manage the contract execution process, including obtaining required signatures and ensuring timely completion.
• Scrutinize contract revisions against negotiation and budget parameters.
• Identify potential contract or process operational risks and collaborate with stakeholders on solutions.
• Track and report on the status of site contracting activities to the Site Contract Lead and study teams.
• Maintain accurate and complete archival records in compliance with company guidelines.

Requirements

• 2-5 years of experience in site contracting or a related field within the CRO industry.
• Bachelor's degree in Law, Economics, Business, Social Sciences, or equivalent industry experience.
• Strong negotiation, diplomacy, and analytical skills.
• Proficiency in MS Office, specifically Excel, Word, and PowerPoint.
• Excellent interpersonal and verbal/written communication skills.
• Ability to work effectively in a virtual team environment.
• High attention to detail and the ability to interpret complex legal language.
• Fluency in written and spoken English.

Benefits

• Flexible work arrangements including home-based or hybrid options.
• Opportunities for professional and personal career development.
• A supportive company culture focused on employee wellness and growth.

About the Company

Parexel is a global leader in clinical research, dedicated to putting patients at the heart of every clinical trial. We combine innovation with expertise to help bring new medical possibilities to life through groundbreaking research and development.