FSP Associate Contract Specialist

Thermo Fisher Scientific

. Draft, review, negotiate and finalize amendments and budgets with study sites .

Posted 10/9/2026full-timeRemote • ArgentinaJuniorMid-LevelWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in drafting, reviewing, and negotiating clinical trial agreements and investigator grant budgets while ensuring compliance with contractual processes and client expectations. Possesses strong analytical skills and effective communication abilities to facilitate collaboration and problem-solving in a team environment.

Highest-signal resume keywords

Clinical Trial AgreementsInvestigator Grant NegotiationContractual ProcessesAnalytical ThinkingEffective Communication

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Budget NegotiationContract ReviewCompliance ManagementTracking and ReportingFinancial PrinciplesAttention to DetailTime ManagementProblem-SolvingAutomated Systems ProficiencyOrganizational Skills

Soft Skills

Effective CommunicationTeam CollaborationIndependent WorkCustomer-Focused CommunicationDecision-Making

Tools & Technologies

PPD SOPWPDsComputerized Applications

Certifications & Qualifications

Bachelor's Degree or Equivalent

Industry Keywords

Clinical TrialsService AgreementsContractual RisksSite ActivationStudy Sites

About the role

Key responsibilities & impact

Draft, review, negotiate and finalize amendments and budgets with study sites
Negotiate investigator grant budgets, contractual terms and conditions within approved parameters
Ensure compliance with negotiation parameters, authority approvals, contractual processes, client expectations, budgetary guidance, templates and procedures
Coordinate with internal functional departments to align site startup and contractual activities with agreed timelines
Ensure contract negotiation activities align with the critical path for site activation
Achieve target cycle times for site activations
Escalate out-of-parameter issues according to established guidelines and processes
Complete required tracking and reporting
Assist other specialists with tracking and reporting

Requirements

What you’ll need

Bachelor's degree or equivalent and relevant formal academic / vocational qualification
Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 0-2 years)
Basic understanding of clinical trial agreements
Basic ability to apply basic principles of investigator grant negotiation
General understanding of business and financial principles related to service agreements
Effective communication skills (verbal & written) in English and local language
Strong attention to detail
Excellent analytical and decision-based thinking
Able to work independently or in a team environment
Good organizational and time management skills
Working knowledge of PPD SOP & WPDs
Able to organize competing priorities logically and review outstanding contractual risks and issues
Able to effectively use automated systems and computerized applications
Ability to demonstrate a customer-focused style of communication, problem-solving and collaboration
Ability to work in an upright and/or stationary position for 6-8 hours per day
Ability to perform repetitive hand movements and frequent mobility
Ability to lift and carry objects up to 15-20 lbs
Regular and consistent attendance