Review, draft and negotiate MSAs, site contracts, vendor and confidentiality agreements.
Coordinate with Clinical Operations to align with study timelines.
Update study teams on contract status and execution.
Establish, track, and report site contract metrics.
Maintain contract files and databases; archiving.
Assist in designing contracting policies to speed execution.

🎯 Requirements

Graduate, postgraduate or 4-year degree.
Experience in CRO/healthcare field.
5+ years drafting, reviewing and negotiating CTAs, vendor contracts, budgets.
Experience leading interactions with study teams and Sponsors.
Preferred: degree in law, science, business or equivalent.
Strong organizational and written communication skills.
Knowledge of contracting plans and CTA budget negotiations.
Proficient in MS Office and document management.

🎁 Benefits

Fully remote in Europe.
Equal Opportunity Employer.

Apply on employer's website

This employer gathers applications via their own applicant tracking system.

You will be redirected to an external application form.

Share job

Meet JobCopilot: Your Personal AI Job Hunter

Automatically Apply to Legal Jobs. Just set your preferences and Job Copilot will do the rest — finding, filtering, and applying while you focus on what matters.

Activate JobCopilot