Global Site Contract Manager

Global Site Contract Manager

Madrid, Spain | Full time | Home-based

Job Overview: As a Global Investigator Contract Manager, you will be responsible for the development of complex investigator grant estimates, contracting strategies, coordination of investigator grants, as applicable and proposal text to support the proposal development process.

You will also develop contract and budget templates and contracting systems, tools, processes, and training materials for selected sponsors and complex studies or multi-protocol programs according to the Scope of Work and Project Plan, within the agreed project strategy, as applicable to the position.

Along with collaborating and communicating with sponsors, stakeholders and RSU regions and countries, to successfully deliver the agreed project scope in compliance with sponsor requirements and/or the RSU Management Plan.

Coupled with being able to provide specialist legal, operational, and financial contracting support to the study teams, as applicable to site agreements to facilitate efficient business development and initiation and maintenance of complex clinical trials, whilst ensuring compliance with regulatory requirements and local laws.

You will create, publish and/or review core scientific, technical, and administrative documentation to support business development and enable study initiation and maintenance, as required. As well as assessing and reviewing the contracting landscape and contribute to the collection, interpretation, analysis, and dissemination of accurate contracting intelligence to support assigned studies and the wider company, as required.

Requirements

• Bachelor’s Degree in Life Science or related field

• 5 years’ relevant sponsor or clinical research organization, clinical site contracting experience, including demonstrable experience acting as an international contract expert

• Strong negotiating and communication skills with ability to challenge

• Ability to coordinate and collaborate across and within complex projects

• Excellent legal, financial and/or technical writing skills

• Thorough understanding of regulated clinical trial environment and knowledge of drug development process

• Knowledge and ability to apply GCP/ICH and applicable regulatory guidelines

• Unleash your potential!

• It takes passion to make the extraordinary possible for patients. Our culture of innovation and collaboration enables us to explore new possibilities and help improve health around the world.

• IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com.