pfm
Senior Contract and Budget Associate
At a Glance
- Location
- United States
- Work Regime
- remote
- Posted
- 2026-03-05T10:17:40-05:00
Key Requirements
Required Skills
Domain Knowledge
- Biotech
- Clinical
- Insurance
- Pharmaceutical
Benefits & Perks
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)