Contract Analyst I

Pharmaceutical Research Associates, Inc; Pistoia; In loco; EUR 45.000 - 60.000; Tempo pieno

Descrizione del lavoro

A leading pharmaceutical company is hiring a Contract Analyst dedicated to managing clinical trial agreements in Italy. The role includes preparing contracts, negotiating terms, and collaborating with teams to ensure compliance with standards. Candidates should possess a Bachelor's degree and relevant experience, offering a chance to impact the pharmaceutical field significantly.

Servizi

Annual leave entitlements

Health insurance options

Global Employee Assistance Programme

Life assurance

Childcare vouchers and gym discounts

Competenze

• 3+ years of experience in legal, pharmaceutical, or clinical research settings.
• Familiarity with healthcare compliance standards is a plus.
• Experience working in virtual teams is preferred.

Mansioni

• Prepare, negotiate, and finalize clinical trial agreements.
• Manage the contract amendment lifecycle.
• Support negotiations of confidentiality agreements.

Conoscenze

Oral Communication

Written Communication

Negotiation

Process Improvement

Database Management

Formazione

Bachelor's degree in a relevant scientific or business field

Strumenti

MS Office

Descrizione del lavoro

We are hiring a Contract Analyst , sponsor dedicated in Italy.

Our client is a pharmaceutical company committed to transforming science into healing to improve lives worldwide.

Would you like to join this team and take your next challenge with ICON Strategic Solutions? Apply today, and we will be happy to discuss this opportunity with you!

Responsibilities

What you will be doing :

• Prepare, negotiate, and finalize clinical trial agreements and ancillary agreements for company-sponsored and investigator-initiated studies through direct negotiation with Clinical Trial Sites.
• Responsible for meeting established targets and measurements.
• Support negotiations of confidentiality agreements, informed consent forms, and other ancillary contract documents as required.
• Participate in developing site / investigator budgets aligned with fair market value.
• Manage the contract amendment lifecycle.
• Collaborate with the global C&G team to review and analyze contractual terms, assess risks, and escalate issues as needed.
• Proactively recommend process improvements to reduce cycle time, create savings, and enhance efficiency in initiating clinical trial sites.
• Track legal documents and metrics.
• Support site payments review and authorization.
• Assist clinical teams in ensuring investigator grants comply with study costs and guidelines.
• Adhere to SOPs, ethics, departmental, and corporate compliance standards.

Qualifications

You are :

• Holding a Bachelor's degree in a relevant scientific or business field.
• Having 3+ years of experience or equivalent competencies in legal, pharmaceutical, or clinical research settings.
• Excellent in oral and written communication.
• Familiar with healthcare compliance standards (HIPAA, FCPA, Safe Harbor, etc.) is a plus.
• Proficient in MS Office and database management.
• Experience working in virtual teams is preferred.

What ICON can offer you :

We value our people and foster a diverse culture that rewards high performance and nurtures talent. In addition to a competitive salary, ICON provides various benefits, including :

• Annual leave entitlements
• Health insurance options
• Global Employee Assistance Programme
• Life assurance
• Optional benefits like childcare vouchers, gym discounts, and more.

Learn more at our careers website :

ICON is committed to inclusion, diversity, and providing an accessible environment for all candidates. We consider all qualified applicants without discrimination. If you require accommodations during the application process, please let us know.

Interested but unsure if you meet all requirements? We encourage you to apply—perhaps you are exactly what we need!

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