Contract Negotiator
6 giorni fa
Milano, Provincia di Milano; Lombardia, Italia
IQVIA
Tempo pieno
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Why Join Clinical Functional Service Partnerships (CFSP)?
At IQVIA, our Clinical Functional Service Partnership (CFSP) models offer the best of both worlds: the opportunity to work as an integrated member of a leading sponsor’s team while benefiting from the global expertise, career development and support of IQVIA. CFSP roles provide the opportunity to develop specialist expertise on a dedicated program, with the flexibility to expand across sponsors and therapeutic areas as your career progresses. Through our long-standing partnerships with top pharmaceutical and biotechnology companies, you will contribute to the delivery of cutting-edge clinical research programs that bring innovative treatments to patients worldwide. Our professionals support studies across all phases of development and a broad range of therapeutic areas, gaining valuable experience in diverse and dynamic research environments. Contract Negotiator At IQVIA, our Contract Negotiators play a critical role in accelerating clinical trial start-up by leading the negotiation, preparation and execution of site agreements and associated legal documents. Working within a sponsor-dedicated environment, you will partner with investigative sites, sponsors, legal teams and cross-functional stakeholders to ensure contracts are negotiated efficiently while maintaining compliance with sponsor requirements and local regulations. As a key contributor to study start-up timelines, you will leverage your negotiation expertise to resolve contractual issues, mitigate risks and drive timely site activation. Backed by IQVIA’s global infrastructure and industry-leading technology, you will gain valuable sponsor-facing exposure and opportunities for long-term career growth within clinical research. Responsibilities- Negotiate clinical trial contracts with research sites, ensuring agreements are completed on time and meet quality and compliance requirements.
- Manage contract changes and additional agreements while balancing business needs and regulatory requirements.
- Support contract planning and study start-up activities for assigned sponsors, studies, and programs.
- Help develop investigator grants, site budgets, contracting plans, and proposal documents.
- Prepare and negotiate contract terms, payment schedules, and budget templates based on project and sponsor needs.
- Work closely with sponsors, stakeholders, and regional study start-up teams to achieve project goals and timelines.
- Provide contract-related guidance and support to study teams on operational and financial matters.
- Gather and share contract and market information to support study planning and decision-making.
- Monitor contract activities to ensure timelines, milestones, and financial goals are met.
- Bachelor’s degree or equivalent.
- 3-5 years of experience in clinical research contract management or a similar role.
- Familiarity with clinical trial processes regulatory requirements and contract lifecycle management.
- Strong analytical organizational and communication skills.