Senior Contracts Manager – FSP

This is a fully remote position, open to applicants in Hungary.

📋 Description

• Review, draft, negotiate, and monitor a diverse range of legal agreements, including confidentiality agreements, master confidentiality agreements, clinical study agreements, and their amendments.

• Collaborate closely with Clinical Operations study teams, playing a vital role in ensuring deliverables align with established study timelines.

• The Senior Contracts Manager will act as a subject matter expert within both the department and the broader company concerning site contract management.

• Develop processes and procedures for comprehensive site contract management within the organization.

• Review, draft, and negotiate various agreements, such as site contracts, confidentiality agreements, and other client contracts.

• Identify and resolve complex issues involving clients and internal stakeholders.

• Negotiate site budgets effectively.

• Provide insights to business teams regarding the operational implications of contract terms.

• Ensure compliance with company policies, procedures, and contracting standards.

• Keep relevant study team members informed about the status of contract negotiations and execution.

• Establish, monitor, report, and manage site contract metrics.

• Oversee the execution of agreements and track expiration dates and other obligations.

• Support the upkeep of contract files and databases, including the archiving of contracts.

• Assist in developing and implementing policies and procedures to ensure the timely execution of contracts.

• Identify areas for process improvement and take corrective measures.

• Mentor and/or serve as an Ambassador for new SCMs and Precision for Medicine staff.

• Perform other responsibilities as assigned.

⛳️ Requirements

• A graduate or postgraduate degree, or a 4-year college degree.

• Equivalent experience, preferably in a scientific or healthcare field.

• Prior experience in a Contract Research Organization (CRO).

• Over 5 years of experience in Oncology.

• Significant experience in drafting, reviewing, and negotiating Clinical Trial Agreements and site budget negotiations, with a minimum of 7 years of relevant experience.

• Proven experience leading interactions with institutions in the US, Europe, APAC, or other regions.

• Skilled in managing interactions with Study Teams and Sponsors.

🏝️ Benefits

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