FSP Associate Contract Specialist

🔥 15 hours ago

🇦🇷 Argentina – Remote

⏰ Full Time

🟢 Junior

🟡 Mid-level

✨ Contract Specialist

👻 Ghost score 10%

What it means: how likely this posting is sitting open without active hiring.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.How we score it: age, reposts, open roles vs team size, how fast jobs close, and whether pay is listed.Fine print: an estimate from public data, not a judgment of the company. Real jobs can score high, so treat it as a hint, not a fact.

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Thermo Fisher Scientific

WebsiteLinkedInAll Job Openings

10,000+ employees

Founded 1956

🏥 Healthcare

📦 Logistics

🏭 Manufacturing

Healthcare • Logistics • Manufacturing

Thermo Fisher Scientific is the world leader in serving science, with annual revenue of more than $40 billion. Their mission is to enable customers to make the world healthier, cleaner, and safer by supporting life sciences research, solving complex analytical challenges, increasing laboratory productivity, and improving patient health through diagnostics and the development of life-changing therapies. With a global team, they offer innovative technologies and pharmaceutical services through brands such as Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services, Patheon, and PPD.

📋 Description

• 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 processes • Coordinate with internal functional departments to align site startup and contractual activities with agreed timelines • Align contract negotiation processes 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

• Bachelor's degree or equivalent and relevant formal academic / vocational qualification • Previous experience comparable to 0-2 years • Equivalency may consist of a combination of appropriate education, training and/or directly related experience • Basic understanding of clinical trial agreements • Basic ability to apply investigator grant negotiation principles • General understanding of business and financial principles related to service agreements • Effective verbal and written communication skills in English and local language • Strong attention to detail • Excellent analytical and decision-based thinking • Ability to work independently or in a team environment • Good organizational and time management skills • Working knowledge of PPD SOP & WPDs • Ability to organize competing priorities and review contractual risks and issues • Ability to use automated systems and computerized applications • Ability to demonstrate customer-focused communication, problem solving and collaboration • Ability to work upright and/or stationary for 6-8 hours per day • Ability to perform repetitive hand movements • Frequent mobility required • Ability to lift and carry 15-20 lbs • Regular and consistent attendance