Sso Contracting Specialist

Novartis; Milano; In loco; EUR 35.000 - 50.000; Tempo pieno

Descrizione del lavoro

A leading pharmaceutical company in Milano is seeking an SSO Contracting Specialist to coordinate clinical study contracts. This role requires strong negotiation skills and at least 1 year of experience in clinical operations. The ideal candidate will have a degree in a scientific or health discipline and knowledge of drug development standards. The position is full-time and offers an engaging work environment.

Competenze

• Qualifications include a degree in a scientific or health discipline.
• At least 1 year of experience in clinical operations or a similar role.
• Understanding of clinical drug development, especially trial setup and contracting.

Mansioni

• Support the country SSU strategy to meet timelines and deliverables.
• Coordinate, prepare, and execute clinical study contracts.
• Negotiate financial and legal terms and track contract statuses.

Conoscenze

Problem-solving

Negotiation

Knowledge of GCP/ICH

Formazione

Degree in a scientific or health discipline

Descrizione del lavoro

387143BR

SSO Contracting Specialist

Location: Italy

About the role

The SSO Contracting Specialist reports to the Study Start Up (SSU) Team Lead and is responsible for coordinating, preparing, and executing clinical study contracts. This role involves close collaboration with SSO Study Start-Up Managers, Clinical Project Managers, and Finance Specialists, ensuring compliance with Novartis processes, GCP/ICH, and regulatory standards.

As an externally facing role, your responsibilities include, but are not limited to:

1. Supporting the country SSU strategy in collaboration with the Study Start-Up Team Lead and Managers to meet timelines and deliverables.
2. Coordinating, preparing, and executing clinical study contracts and amendments.
3. Negotiating financial and legal terms, escalating issues as needed, and tracking contract statuses.
4. Ensuring compliance with financial standards, legislation, ICH/GCP, IRB/IEC, Health Authorities, and SOPs.
5. Implementing innovative and efficient processes aligned with Novartis strategy.
6. Promoting diversity and inclusion within the team.

Role Requirements

Qualifications include a degree in a scientific or health discipline, with preferable experience in clinical operations or project management.

Experience / Professional Requirements:

• At least 1 year of experience in clinical operations or a similar role.
• Understanding of clinical drug development, especially trial setup and contracting.

Competencies:

• Strong problem-solving and mediation skills.
• Knowledge of international drug development standards (GCP/ICH), health authorities (FDA/EMEA), and local regulations.

Additional Information

• Division: Global Drug Development
• Business Unit: GCO GDD
• Location: Milano
• Company: Novartis Farma IT
• Area: Research & Development
• Job Type: Full Time
• Employment Type: Regular
• Shift Work: No
• Early Talent: No

This job posting is active and accepting applications.