Contract Negotiator 2 - FSP - German speaker

IQVIA; Basel; Vor Ort; CHF 90’000 - 120’000; Vollzeit

Zusammenfassung

A leading global provider of clinical research services seeks a professional to coordinate and manage clinical trial site contracting. This role emphasizes legal and financial support while ensuring compliance with regulatory standards. Candidates should have a Bachelor's degree and strong negotiating skills, along with fluency in English and German.

Qualifikationen

• 5 years of relevant sponsor or CRO clinical site contracting experience.
• Strong legal, financial, and technical writing skills.

Aufgaben

• Coordinate development of investigator grants and contracts.
• Provide legal and financial support to Study Teams.
• Ensure adherence to contracting timelines and financial goals.

Kenntnisse

Negotiating skills

Communication skills

Legal writing skills

Technical writing skills

Regulatory compliance knowledge

Contract management knowledge

Fluency in English

Fluency in German

Ausbildung

Bachelor's Degree in a related field

Jobbeschreibung

Responsibilities:

1. Coordinate the development of investigator grants, estimates, contracting strategies, and proposal text 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 for sponsors, studies, or multi-protocol programs according to the Scope of Work and Project Plan.
4. Communicate and collaborate with sponsors, stakeholders, and RSU regions and countries to deliver project scope in compliance with sponsor requirements and RSU Management Plan.
5. Provide legal, operational, and financial contracting support to Study Teams for site agreements, facilitating efficient business development and trial initiation, ensuring regulatory compliance.
6. Ensure contracting efficiency, adherence to timelines, and financial goals related to site agreements.
7. Report on contracting performance metrics and out-of-scope activities as needed.
8. Work with Quality Management to uphold contract management and quality standards. Mentor colleagues and deliver training as required.

Qualifications:

1. Bachelor's Degree in a related field or 5 years of relevant sponsor or CRO clinical site contracting experience.
2. Excellent negotiating and communication skills, with the ability to challenge appropriately.
3. Strong legal, financial, and technical writing skills.
4. Deep understanding of the regulated clinical trial environment and drug development process.
5. Knowledge of clinical trial contract management.
6. Fluent in English and German.

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 medical treatments to improve patient outcomes and population health worldwide. Learn more at IQVIA's official website.