Site Contract Specialist

🔥 44 minutes ago

🇹🇷 Turkey – Remote

⏰ Full Time

🟡 Mid-level

🟠 Senior

✨ Contract Specialist

👻 Ghost score 10%

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Logo of Thermo Fisher Scientific

Thermo Fisher Scientific

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 agreements 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 • Identify and assess legal, financial and operational risks and escalate issues appropriately • Provide recommendations and alternative resolutions for Investigator Contracts negotiations • Coordinate with internal functional departments to align site startup and contractual activities with agreed timelines and site activation critical paths • Achieve target cycle times for site activations • Track and report activities as required • Train and mentor junior staff • Participate in country process improvement initiatives and country team meetings • Act as country subject matter expert for Investigator Contracts training materials • Liaise with Global Site Contracts to ensure compliance with global processes and corporate directives • Complete periodic quality reviews and peer feedback reports • Lead amendment/novation client projects and oversee confidentiality agreement negotiations when applicable

🎯 Requirements

• Bachelor's degree or equivalent and relevant formal academic/vocational qualification • 5+ years of comparable experience providing the knowledge, skills, and abilities to perform the job • Combination of appropriate education, training and/or directly related experience may be considered sufficient • Detailed understanding of contract law, including business, intellectual property, local tax and stamp laws • Effective verbal and written communication skills in English and the local language • Ability to negotiate investigator grant budgets within approved parameters • Strong attention to detail • Excellent analytical and decision-based thinking skills • Knowledge of pharmaceutical product development processes and CRO involvement • Ability to work independently and in a team environment • Organizational and time management skills • Working knowledge of PPD SOPs and WPDs • Ability to organize competing priorities and review contractual risks and issues • Ability to use automated systems and computerized applications • Customer-focused communication, problem solving and collaboration skills • Ability to train and mentor staff independently • Ability to provide valuable feedback to Investigator Analysts • Strong problem-solving and risk-analysis skills • Ability to negotiate Investigator Contracts in the best interests of the company and client

🏖️ Benefits

• Fully remote work arrangement • Standard Monday–Friday work schedule • Training and mentoring opportunities • Collaboration and professional development within a global team • Meaningful work contributing to life-changing therapies and improved health outcomes

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