Precision Medicine Group

Senior Contracts and Budget Associate

Full-time3+ yrsSouth KoreaNot disclosedApply by 16 Oct 2026
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WA

Overview

Position Summary: Review, draft, negotiate and track a variety of legal agreements including confidentiality disclosure agreements (CDA), initial clinical trial agreements (CTA), amendments to the clinical trial agreements (CTA-A), site budgets and other various types of documents. Will work closely with the Clinical Operations study team and play an administrative role to ensure deliverables are

What you'll do

  • Position Summary: Review, draft, negotiate and track a variety of legal agreements including confidentiality disclosure agreements (CDA), initial clinical trial agreements (CTA), amendments to the clinical trial agreements (CTA-A), site budgets and other various types of documents.
  • Will work closely with the Clinical Operations study team and play an administrative role to ensure deliverables are in alignment with defined project timelines and expectations.
  • Essential functions of the job include but are not limited to: • 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 interactions with the North American and European internal study teams, as applicable • Lead interactions regarding the various agreements with the Site(s) • Lead interactions regarding assigned agreements with the Sponsor(s) • Work with supervisor and various internal/external stakeholders to resolve contractual issues.
  • • Ensure adhered to company policies, procedures, and contracting standards.
  • • Update relevant study team members and sponsors regarding the status of contract negotiations and execution.
  • • Coordinate execution of the agreements • Support the maintenance of contract files and databases, including email and document archiving.
  • • Other duties as assigned.
  • Qualifications: Minimum Required: • Bachelor’s degree, or equivalent contract management experience preferably in a clinical research or similar industry setting Other Required: • 3 years of relevant experience drafting, reviewing and negotiating agreements related to clinical research i.e.
  • Non-Disclosure Agreements, Clinical Trial Agreements, etc.

Requirements

  • Practical experience with supervisor, customer support, exec, senior.
  • Experience level: 3+ yrs.
  • Strong written and verbal communication in English.
  • Comfortable working on-site in South Korea.

Skills

supervisorcustomer supportexecsenioropslegalbiotech

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