Senior Contracts and Budget Associate

This is a fully remote position, open to applicants in South Korea.

📋 Description

• Review, draft, negotiate, and monitor a variety of legal agreements, including confidentiality disclosure agreements (CDA), initial clinical trial agreements (CTA), amendments to clinical trial agreements (CTA-A), site budgets, and other diverse document types.

• Collaborate closely with the Clinical Operations study team, taking on an administrative role to ensure that deliverables align with established project timelines and expectations.

• Prepare and negotiate agreements/amendments such as Confidentiality Disclosure Agreements (CDA), Clinical Trial Agreements (CTA), and Amendments (CTA-A), vendor contracts, and site budgets.

• Lead communications with internal study teams in North America and Europe, as applicable.

• Facilitate discussions regarding various agreements with the Site(s).

• Manage interactions concerning assigned agreements with the Sponsor(s).

• Collaborate with supervisors and various internal/external stakeholders to address contractual issues.

• Ensure compliance with company policies, procedures, and contracting standards.

• Provide updates to relevant study team members and sponsors about the status of contract negotiations and execution.

• Coordinate the execution of agreements.

• Assist in maintaining contract files and databases, including email and document archiving.

• Perform other duties as assigned.

⛳️ Requirements

• Bachelor’s degree or equivalent experience in contract management, preferably within a clinical research or similar industry setting.

• A minimum of 3 years of relevant experience in drafting, reviewing, and negotiating agreements related to clinical research, such as Non-Disclosure Agreements and Clinical Trial Agreements, along with managing, controlling, and tracking the contract process.

• Preferred experience in contract research, life sciences, biotech, or the pharmaceutical industry.

• Equivalent experience in contract management within clinical research or a related industry setting.

• Background in contract research, life sciences, biotech, or the pharmaceutical industry is preferred.

🏝️ Benefits

• No explicit benefits mentioned in the job description.