Contract Negotiator FSP

IQVIA; Barcelona; Híbrido; EUR 40.000 - 55.000; Jornada completa

Descripción de la vacante

Join a leading global provider in clinical research as a Clinical Research Associate. You'll support contracting activities for studies, ensuring compliance while collaborating with sponsors. This role offers the chance to work on innovative medicines and develop your career in a dynamic environment.

Servicios

Career development opportunities

Opportunity to work on cutting-edge medicines

Formación

• At least 3 years of relevant sponsor or CRO clinical site contracting experience.
• Strong negotiating and communication skills.

Responsabilidades

• Coordinate development of investigator grants and contracting strategies.
• Provide legal, operational, and financial contracting support.
• Report on contracting performance metrics.

Conocimientos

Negotiating

Communication

Legal Writing

Technical Writing

Educación

Bachelor's Degree

Descripción del empleo

Remote / Hybrid / Office based working options.

Our Sponsor Dedicated (cFSP) team is growing. Join us on our mission to drive healthcare forward! As a Clinical Research Associate, you will develop the local contracting strategy and support the delivery of all required start-up contracting activities for selected sponsors, studies, or multi-protocol programs as determined by the Sponsor’s requirements.

Job Overview :

1. Coordinate the development of investigator grants, estimates, contracting strategies, and proposal texts to support proposal development.
2. Develop contract language, payment language, and budget templates as applicable.
3. Utilize and maintain contracting systems, tools, processes, and training materials according to the Scope of Work and Project Plan.
4. Collaborate with sponsors, stakeholders, and RSU regions and countries to deliver the project scope in compliance with sponsor requirements and the RSU Management Plan.
5. Provide legal, operational, and financial contracting support to Study Teams to facilitate efficient business development and trial initiation, ensuring regulatory compliance.
6. Contribute to collecting, interpreting, analyzing, and disseminating contracting intelligence to support studies and the wider company.
7. Ensure contracting efficiency and adherence to timelines and financial goals.
8. Report on contracting performance metrics and out-of-scope activities.
9. Work with Quality Management to ensure standards; mentor colleagues and deliver training as needed.

Requirements :

1. Bachelor's Degree in a related field.
2. At least 3 years of relevant sponsor or CRO clinical site contracting experience, including global or regional negotiation experience, or equivalent education, training, and experience.
3. Strong negotiating and communication skills, with the ability to challenge.
4. Legal, financial, and technical writing skills.
5. Understanding of clinical trial contract management.
6. Ability to use metrics to communicate timelines and deliverables.

What is in it for you?

• Opportunity to work on cutting-edge medicines at the forefront of new development.
• Genuine career development opportunities within the organization.

IQVIA is a leading global provider of analytics, technology, and clinical research services to the life sciences industry. We aim to push the boundaries of human and data science to make a significant impact—helping our clients create a healthier world. Learn more at IQVIA.