Contract Negotiator FSP

TN Germany; Bochum; Hybrid; EUR 50.000 - 90.000; Vollzeit

Zusammenfassung

An innovative firm is seeking a Clinical Research Associate to join their expanding team dedicated to advancing healthcare. In this role, you will develop local contracting strategies and support essential start-up activities for various studies. You'll collaborate with sponsors and stakeholders to ensure compliance and efficiency in contract management. This position offers you the chance to work on groundbreaking medicines while providing genuine career development opportunities within a leading organization in clinical research services. If you're passionate about making a significant impact in the life sciences industry, this role is perfect for you.

Leistungen

Career Development Opportunities

Remote Working Options

Cutting-edge Medicine Projects

Qualifikationen

• 3+ years of experience in clinical site contracting.
• Strong negotiation and communication skills essential.

Aufgaben

• Coordinate investigator grants and contracting strategies.
• Provide legal and financial support for site agreements.

Kenntnisse

Negotiation Skills

Communication Skills

Legal Writing

Financial Writing

Clinical Trial Management

Ausbildung

Bachelor's Degree

Jobbeschreibung

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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.