Global Clinical Trials Contracts & Budget Lead

IQVIA; Barcelona; Presencial; EUR 70.000 - 110.000; Jornada completa

Descripción de la vacante

IQVIA in Barcelona, Spain is seeking a professional to oversee clinical trial budgets and lead global negotiation activities. You will manage contracts with sites and sponsors, coordinate timelines, and develop contracting strategies to support large-scale trials.

The role requires a degree in science or healthcare, 3–5 years of relevant experience, and strong negotiation and communication skills. You will work with cross-functional teams to ensure compliant, timely outcomes.

Formación

• Bachelor’s Degree in Scientific discipline or Healthcare.
• 3 to 5 years prior relevant experience.
• Good negotiating and communication skills with ability to challenge.
• Thorough understanding of regulated clinical trial environment and knowledge of drug development process.
• Goal oriented, self-starter with proven ability to work independently.

Responsabilidades

• Preparation, review, negotiation and management of clinical trial agreements with sites and sponsors.
• Serves as the primary point of contact for investigative sites and/or sponsors.
• Ensures tracking completion of all contractual documents for sites.
• Establishes project timelines.
• Establishes and/or executes goals and objectives for team(s) as well as tracking and delivering on operational/financial performance.
• Responsible for the development of complex contracting strategies, coordination of investigator grants, as applicable and proposal text to support the proposal development process.
• Develop contract and budget templates and contracting systems, tools, processes, and training materials.

Conocimientos

Budget negotiation

Contract management

Clinical trials

Regulatory knowledge

Stakeholder management

Educación

Bachelor’s Degree in Scientific discipline or Healthcare

Descripción del empleo

IQVIA in Barcelona, Spain is seeking a professional to oversee clinical trial budgets and lead global negotiation activities. You will manage contracts with sites and sponsors, coordinate timelines, and develop contracting strategies to support large-scale trials.

The role requires a degree in science or healthcare, 3–5 years of relevant experience, and strong negotiation and communication skills. You will work with cross-functional teams to ensure compliant, timely outcomes.