pfm

Senior Contract and Budget Associate

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At a Glance

Location
United States
Work Regime
remote
Posted
2026-03-05T10:17:40-05:00

Key Requirements

Required Skills

Microsoft Office

Domain Knowledge

  • Biotech
  • Clinical
  • Insurance
  • Pharmaceutical

Benefits & Perks

Health Insurance

onary annual bonus, health insurance, retirement savings benefits, life insu

Requirements

research or similar industry setting

3 years of relevant experience drafting, reviewing and negotiating agreements related to clinical research i.e.

Non-Disclosure Agreements, Clinical Trial Agreements, etc.

Experience in tracking status for site contracts and budget, filing and distribution.

Demonstrates a high degree of professionalism, as evidenced by punctuality, ability to deliver on commitments and understanding of the service culture and positive interactions with customers.

Reasonable estimate of the current range

Responsibilities

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.

Prepare and negotiate Agreements/Amendments such as Confidentiality Disclosure Agreements (CDA), Clinical Trial Agreements (CTA) and Amendments (CTA-A), vendorcontracts 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)