Contract Negotiator FSP

IQVIA; Bochum; Hybrid; EUR 50.000 - 80.000; Vollzeit

Zusammenfassung

An innovative firm is seeking a Clinical Research Associate to join their growing team. This role involves developing local contracting strategies and supporting start-up activities for clinical trials. You will collaborate with various stakeholders to ensure project delivery while maintaining compliance with sponsor requirements. The position offers the chance to work on cutting-edge medicines, providing genuine career development opportunities within a leading global provider of analytics and clinical research services. If you are passionate about advancing healthcare and have strong negotiation skills, this is the perfect opportunity for you.

Leistungen

Career Development Opportunities

Work on Cutting-Edge Medicines

Qualifikationen

• 3+ years of clinical site contracting experience with strong negotiation skills.
• Ability to manage contracting efficiency and compliance with timelines.

Aufgaben

• Coordinate development of investigator grants and contracting strategies.
• Provide legal and financial support to Study Teams for trial initiation.

Kenntnisse

Negotiation Skills

Communication Skills

Contract Management

Technical Writing

Ausbildung

Bachelor's Degree in a related field

Jobbeschreibung

Remote / Hybrid / Office based working options.

Our Sponsor Dedicated (cFSP) team is growing. Join us on our mission to advance healthcare! As a Clinical Research Associate, you will develop local contracting strategies and support the delivery of start-up contracting activities for selected sponsors, studies, or multi-protocol programs based on sponsor 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 terms, 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 to ensure successful project delivery in compliance with sponsor requirements and RSU Management Plan.
5. Provide legal, operational, and financial contracting support to Study Teams, focusing on site agreements to facilitate efficient trial initiation and compliance.
6. Contribute to collecting, analyzing, and disseminating contracting intelligence to support studies and the company.
7. Ensure contracting efficiency, adherence to timelines, and financial goals.
8. Report on contracting performance and out-of-scope activities.
9. Work with Quality Management to maintain standards; mentor colleagues and deliver training as needed.

Requirements:

• Bachelor's Degree in a related field.
• At least 3 years of sponsor or CRO clinical site contracting experience, including global or regional negotiation experience. Equivalent education, training, and experience are acceptable.
• Strong negotiation and communication skills, with the ability to challenge appropriately.

Additional Skills:

• Strong legal, financial, and technical writing skills.
• Good understanding of clinical trial contract management.
• Ability to use metrics to communicate timelines and deliverables with study teams.

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 solutions, and clinical research services to the life sciences industry. We aim to push the boundaries of human and data science to create a healthier world. Learn more at