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

📋 Description

• Review, draft, negotiate, and monitor confidentiality agreements, master confidentiality agreements, clinical study agreements, and amendment agreements.

• Review, draft, and negotiate master services agreements, site contracts, consulting agreements, vendor agreements, confidentiality agreements, and other client contracts.

• Collaborate with supervisors and internal/external stakeholders to address or escalate contractual issues.

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

• Update study team members regarding the status of contract negotiations and executions.

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

• Support the maintenance and archiving of contract files and databases.

• Assist in the design and implementation of procedures for timely contract execution.

• Identify opportunities for process improvements and take corrective actions.

• Perform additional assigned tasks.

⛳️ Requirements

• Bachelor's degree, graduate, or postgraduate qualification from a four-year college.

• Experience in a CRO or healthcare environment.

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

• Experience leading interactions with Study Teams and Sponsors.

• Proficiency in MS Office software applications and computer programs.

• Ability to work both independently and collaboratively within a team.

• Excellent organizational and written communication skills.

• Ability to multitask and prioritize effectively in a fast-paced environment.

• Capability to manage time-sensitive matters accurately while paying attention to detail.

• Ability to handle sensitive issues with discretion.

• Candidates must be legally authorized to work in the country of employment without requiring employer sponsorship.