Contract Negotiator (FSP) France

IQVIA; France; Sur place; EUR 50 000 - 70 000; Plein temps

Résumé du poste

A leading global clinical research provider is seeking a professional to develop the global contracting strategy, support site agreements, and ensure compliance with sponsor requirements. Candidates should have a Bachelor's degree and at least 5 years of relevant clinical site contracting experience. Strong negotiation, interpersonal, and organizational skills are required for this role based in France. Competitive package and opportunities for career development are offered.

Qualifications

• 5 years of experience in clinical site contracting, including as a negotiator.
• Strong knowledge of the regulated clinical trial environment.
• Experience in establishing effective working relationships.

Responsabilités

• Develop the global contracting strategy and support contracting activities.
• Ensure compliance with sponsor requirements for clinical trials.
• Provide legal and financial contracting support for study teams.

Connaissances

Negotiating skills

Interpersonal skills

Technical writing

Knowledge of GCP/ICH

Organizational skills

Presentation skills

Formation

Bachelor's Degree in a related field

Outils

Microsoft Office

Description du poste

Job Overview
Develop the global contracting strategy and support the delivery of all required start-up contracting activities for selected sponsors, studies or multi-protocol programs as determined by the Sponsor’s requirements.

Essential Functions

• Develop Coordinate the development of investigator grants and estimates, contracting strategies and proposal text to support the proposal development process.
• Develop contract language, payment language and budget templates as required as applicable to the position
• Utilize and maintain contracting systems, tools, processes, and training materials for selected sponsors, studies or multi-protocol programs according to the Scope of Work and Project Plan, within the agreed project strategy.
• Ensure collaboration, including communication with sponsors, stakeholders and RSU regions and countries as applicable to the position, to successfully deliver the agreed project scope in compliance with sponsor requirements and/or the RSU Management Plan.
• 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 clinical trials, whilst enabling compliance with regulatory requirements.
• Assist with the creation and/or review of core scientific, technical and administrative documentation to support business development and enable study initiation and maintenance, as required.
• Contribute to the collection, interpretation, analysis and dissemination of accurate contracting intelligence to support assigned studies and the wider company, as required.
• Ensure overall contracting efficiency and adherence to project timelines and financial goals as applicable to site agreements
• Report contracting performance metrics and out of scope contracting activities as required.
• Work with Quality Management to ensure appropriate contract management and quality standards. Mentor and coach colleagues as required including the delivery of training materials as required.
• Deliver presentations to clients as required. As applicable, eEnsure accurate completion and maintenance of internal systems (with emphasis on CTMS), databases, tracking tools, timelines and project plans.
• May take a proactive role in developing long standing relationships with preferred IQVIA clients/customers.

Qualifications
Bachelor's Degree Related field Req
5-year relevant sponsor or clinical research organization clinical site contracting experience, including demonstrable global and/ore regional experience acting as a contract negotiator. Equivalent combination of education, training and experience.

• Good negotiating and communication skills with ability to challenge.
• Good interpersonal skills and a strong team player.
• Strong legal, financial and/or technical writing skills.
• Strong understanding of regulated clinical trial environment and knowledge of drug development process.
• Knowledge and ability to apply GCP/ICH and applicable regulatory guidelines.
• Knowledge of applicable regulatory requirements, SOPs and company’s Corporate Standards.
• Ability to exercise independent judgment, taking calculated risks when making decisions.
• Ability to lead, motivate, coach and mentor.
• Good organizational and planning skills.
• Good presentation skills.
• Strong knowledge of Microsoft Office and e-mail applications.
• Good understanding of clinical trial contract management.
• Ability to work well within a matrix team environment.
• Ability to establish and maintain effective working relationships with co-workers, managers and sponsors.
• Ability to develop and suggest alternate contracting language, terms, and financial options.
• Strong understanding of particular Sponsor or stakeholder need and ability to share this knowledge effectively with others.
• Ability to utilize metrics and then communicate these with study team to establish timelines for deliverables.

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