This is a fully remote position, open to applicants in Slovakia, +4 more countries.

📋 Description

• Review, draft, negotiate, and monitor legal agreements such as confidentiality agreements, master services agreements, clinical study agreements, site contracts, consulting agreements, vendor agreements, amendments, and other client contracts.

• Address or escalate contractual issues with supervisors and both internal and external stakeholders.

• Ensure adherence to company policies, procedures, and contracting standards.

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

• Establish, monitor, report, and manage metrics related to site contracts.

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

• Assist in designing and implementing processes for timely contract execution.

• Identify opportunities for process improvements and take corrective actions as necessary.

• Collaborate with Clinical Operations study teams to ensure deliverables align with study timelines.

• Carry out other assigned tasks.

⛳️ Requirements

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

• Experience in a CRO or healthcare environment.

• A minimum of 5 years of pertinent experience in drafting, reviewing, and negotiating site Clinical Trial Agreements, Vendor Contracts, and Site Budget negotiations.

• Experience in leading interactions with Study Teams and Sponsors.

• Proficiency in MS Office software applications and other computer programs.

• Legal authorization to work in the country of employment without requiring employer sponsorship.