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

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

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

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

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

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

• Support the design and implementation of policies and procedures to ensure timely contract execution.

• Identify opportunities for process improvements and take corrective actions.

• Perform additional assigned tasks.

⛳️ Requirements

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

• Experience in a CRO or healthcare setting.

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

• Proven experience leading interactions with Study Teams and Sponsors.

• Proficient in MS Office software programs and computer applications.

• Must be legally authorized to work in the country of employment without sponsorship from the employer.

• Strong organizational skills and written communication abilities.

• Capable of multitasking, prioritizing, and accurately managing time-sensitive matters.

• Ability to work independently as well as collaboratively in a team environment.

• Preferred knowledge of contract plans/guides for Clinical Trial Agreement and budget negotiations.

• A bachelor's degree in law, scientific fields, or business administration is preferred.