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

📋 Description

• Assess, create, negotiate, and monitor various legal contracts, including confidentiality agreements, master confidentiality agreements, clinical study agreements, and their amendments.

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

• Act as a subject matter expert within the department and across the company concerning site contract management.

⛳️ Requirements

• Bachelor's degree or higher, including postgraduate qualifications.

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

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

• Over 5 years of experience in Oncology.

• Relevant background in drafting, reviewing, and negotiating site Clinical Trial Agreements and site Budget negotiations, with a minimum of 7 years of experience.

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

• Demonstrated ability in managing interactions with Study Teams and Sponsors.