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Clinical Contracts Associate

Pubblicato il 10-09-2026 - Kelly Science, Engineering, Technology & Telecom in Reggio Emilia

Clinical Contracts Associate – Italy

Location: Remote, Italy – open to candidates based anywhere in Italy
Employment Type: Full-Time, 12-Month Fixed-Term Contract
Hours: 40 hours per week
Start Date: To be confirmed
Project Status: Pipeline opportunity, pending final client approval
Client: Leading Global Medical Device Organisation

About the Role:

We are currently building a pipeline for an exciting opportunity with a leading global medical device organisation for a Clinical Contracts Associate – Italy.

This role will support clinical research activities across the EMEA region, with responsibility for the preparation, review, negotiation and execution of clinical trial contracts, budgets and related amendments.

Working with clinical, legal, compliance and other cross-functional stakeholders, the Clinical Contracts Associate will help ensure agreements are commercially appropriate, aligned with clinical study requirements and compliant with applicable regulations and company policies.





The successful candidate will have strong experience in clinical contracting within the medical device industry and be comfortable working independently in a complex, international and highly matrixed environment.

Please note: This opportunity is currently in the project pipeline and is pending final client go-ahead. The role will be fully remote for candidates based anywhere in Italy.

Key Responsibilities
- Prepare, review, negotiate and execute clinical trial contracts, budgets, amendments, work orders, modifications and change orders across the EMEA region.
- Adapt study site budget templates to meet country-specific and site-specific requirements.
- Review clinical agreements and associated documentation to identify potential corporate, legal and commercial risks.
- Develop appropriate approaches to mitigate identified contractual risks in collaboration with relevant stakeholders.
- Negotiate directly with research sites and other external parties regarding contract terms a

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