Contract Analyst I

ICON; Biella; In loco; EUR 40.000 - 65.000; Tempo pieno

Descrizione del lavoro

A leading company in the pharmaceutical industry is seeking a Contract Analyst to prepare and finalize clinical trial agreements. Ideal candidates will have a Bachelor’s degree, 3 years of relevant experience, and excellent communication skills. The role includes managing contracts and collaborating with global teams to ensure compliance and efficiency in trial processes.

Servizi

Various annual leave entitlements

Health insurance offerings

Competitive retirement planning offerings

Global Employee Assistance Programme

Life assurance

Flexible optional benefits

Competenze

• 3 years experience in legal/pharmaceutical industry/clinical research.
• Familiarity with healthcare compliance (HIPAA, FCPA) a plus.
• Previous experience working in virtual teams preferred.

Mansioni

• Prepare, negotiate, and finalize clinical trial agreements.
• Responsible for delivery against established targets.
• Manage the contract amendment lifecycle.

Conoscenze

Excellent communication skills

Fluency in English

Formazione

Bachelor's degree in appropriate scientific or business discipline

Strumenti

MS Office suite

Descrizione del lavoro

We are hiring a Contract Analyst , sponsor dedicated in Italy

Our client isa medicine company turning science into healing to make life better for people around the world.

Would you like to become part of this team and take your next challenge with ICON Strategic Solutions?

Apply today and we'll be happy to discuss this opportunity with you!

What you will be doing :

• Prepare, negotiate, and finalize clinical trial agreements and ancillary agreements for company sponsored and / or investigator initiated studies through direct negotiation with Clinical Trial Sites.
• Responsible for delivery against established targets / measurements.
• Provide support for negotiations in confidentiality agreements, informed consent forms and other ancillary contract documents as required.
• Participate in discussions related to the development of site / investigator budgets aligned with fair market value.
• Manage the contract amendment lifecycle.
• Work with the global C&G team as necessary to review and analyse contractual terms to reach resolution. Assess risks of budget and legal provisions in conjunction with members of the C&G team and support functions. Escalate issues as appropriate.
• Work proactively to provide recommendations to improve processes and establish refinements that reduce cycle time, create savings and improve efficiency in the initiation of clinical trial sites.
• Assume responsibility for all aspects of legal document and metrics tracking.
• Provide support to review, authorize and / or understand aspects of site payments.
• Assist clinical operations or clinical team in ensuring that investigator grants comply with overall study costs and compliance guidelines.
• Adhere to SOPs, ethics and departmental compliance as determined by departmental management as well as operating companies, corporate, HCC and QA guidelines. Ensure familiarity with departmental and appropriate corporate processes.
• Comply with requests from QA and auditors.

You are :

• Bachelor's degree in appropriate scientific or business discipline
• 3 years experience and / or equivalent competencies in legal / pharmaceutical industry / clinical research
• Excellent communication skills (both oral and written)
• Familiarity with healthcare compliance and other relevant guidance (HIPAA, FCPA, Safe Harbor, etc.) a plus
• Working knowledge of PCs (MS Office suite at a minimum) and database management
• Fluency in English is required
• Previous experience working in virtual teams preferred

What ICON can offer you :

Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.

In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.

• Various annual leave entitlements
• A range of health insurance offerings to suit you and your family’s needs
• Competitive retirement planning offerings to maximise savings and plan with confidence for the years ahead
• Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family’s well-being
• Life assurance
• Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others

Visit our careers website to read more about the benefits of working at ICON : ICON, inclusion & belonging are fundamental to our culture and values. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, colour, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know through the form below.

in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles.

J-18808-Ljbffr