Senior Contracts and Budget Associate – FSP

Precision For Medicine

Senior Contracts and Budget Associate managing legal agreements including confidentiality and clinical trial agreements. Collaborating with cross-functional teams to ensure project timelines and expectations.

Posted 7/10/2026full-timeRemote • 🇺🇸 United StatesSenior💰 $68,700 - $103,700 per yearWebsite

Core Competencies

Role fit

Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates expertise in drafting, reviewing, and negotiating legal agreements within the clinical research sector, with a strong focus on compliance with company policies and effective stakeholder communication.

Highest-signal resume keywords

Contract DraftingClinical Trial Agreements (CTA)Confidentiality Disclosure Agreements (CDA)Negotiation SkillsContract Management

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Agreement ReviewContract NegotiationDocument TrackingSite Budget ManagementAmendment Preparation

Soft Skills

CommunicationCollaborationProblem-Solving

Tools & Technologies

Contract DatabasesEmail Archiving

Industry Keywords

Clinical ResearchBiotechPharmaceuticalLife SciencesEuropean Institutions

About the role

Key responsibilities & impact

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), 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.

Requirements

What you’ll need

Bachelor’s degree, or equivalent contract management experience preferably in a clinical 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. as well as management, control and tracking of the contract process.
Experience in contract research, life science, biotech or pharmaceutical industry is preferred.
Experience interacting with European institutions.

Benefits

Comp & perks

discretionary annual bonus
health insurance
retirement savings benefits
life insurance and disability benefits
parental leave
paid time off for sick leave and vacation