Senior Contracts and Budget Associate - FSP
Precision Medicine Group · United States · US
Clinical Research
Remote
Not yet analysed
Demand72
Career growth68
Healthcare fit60
Remote potential75
Salary band
USD 69k – 103k
5-year outlook
Stable upward progression is plausible from senior contracts/budget associate to contract or budget manager, site contracts lead, or clinical operations roles in CRO/FSP settings; exact salary growth depends on sponsor-facing experience, location, and company.
Clinical license
Not required
Applicant reach
moderate
Seniority
senior
Employment type
full-time
Date found
2026-10-29
Intelligence details
Flexible work details
- Engagement type
- Contract
- Hours
- Variable hours
- Eligible countries
- United States
- Rate period
- Annual
Why this was classified this way
- contract
Listing via Himalayas.
Eligibility, licensing, and location restrictions can change. Always confirm details on the source posting before applying.
Why this is worth applying to
Worth considering if you already have clinical research site, study start-up, contracts, or budget exposure and want a non-clinical CRO/FSP pathway; less suitable for clinicians without direct contract negotiation experience.
Who should apply
Clinicians with clinical trial coordination, site research, study start-up, contracts, or budget experience; nurses or doctors transitioning from site-based research; healthcare graduates with CRO, pharma, or contract management exposure.
CV angle
Frame real clinical research experience around study start-up, site communication, budget tracking, confidentiality and regulatory documents, stakeholder coordination, and timeline management; quantify numbers of studies, sites, agreements, or budgets supported without inventing contract negotiation experience.
Skills to highlight
- clinical trial agreements
- contract tracking
- site budgets
- stakeholder communication
- clinical operations
- document management
- attention to detail
- MS Office
Role summary
A clinical research contracts and budgets role focused on preparing, negotiating, tracking, and executing CDAs, clinical trial agreements, amendments, vendor contracts, and site budgets while coordinating with internal study teams, sites, and sponsors.
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