Contract Negotiator FSP

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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 according to the Sponsor’s requirements.

Job Overview:

1. Coordinate the development of investigator grants, estimates, contracting strategies, and proposal text to support the proposal development process.
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. Ensure collaboration and communication 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 for site agreements, facilitating efficient business development and trial initiation while ensuring regulatory compliance.
6. Contribute to the collection, interpretation, analysis, and dissemination of contracting intelligence to support studies and the wider company.
7. Ensure contracting efficiency and adherence to timelines and financial goals related to site agreements.
8. Report on contracting performance metrics and out-of-scope activities.
9. Work with Quality Management to ensure contract management standards. Mentor and train colleagues as needed.

Requirements:

• Bachelor's Degree in a related field.
• At least 3 years of relevant sponsor or CRO clinical site contracting experience, including global or regional experience as a contract negotiator. An equivalent combination of education, training, and experience is acceptable.
• Strong negotiating and communication skills, with the ability to challenge and influence.
• Excellent legal, financial, and technical writing skills.
• Good understanding of clinical trial contract management.
• Ability to utilize metrics and communicate timelines and deliverables effectively.

What is in it for you?

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

IQVIA is a leading global provider of analytics, technology solutions, and clinical research services to the life sciences industry. We are committed to advancing human science and data science to make a significant impact—helping our customers create a healthier world. Learn more at our website.