26 ott - Lombardia
Iqvia
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.
Associate Clinical Operations Manager
At IQVIA, our Associate Clinical Operations Manager 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,
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