This is a fully remote position, open to applicants in Spain, +5 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 various client contracts.

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

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

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

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

• Assist in the maintenance and archiving of contract files and databases.

• Help design and implement procedures for timely contract execution.

• Identify opportunities for process improvements and take corrective actions.

• Perform other assigned tasks.

⛳️ Requirements

• Graduate, postgraduate, or a 4-year college degree.

• Experience in a CRO or healthcare field.

• A minimum of 5 years’ 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.

• Preferred: Bachelor's degree in law, scientific fields, business administration, or an equivalent discipline.

• Preferred: Familiarity with establishing Contracting Plans and guides for CTA and budget negotiations.

• Proficiency in MS Office software programs and computer applications.

• Capacity to handle sensitive issues with discretion.

• Ability to work both independently and collaboratively in a virtual environment.