Financial Clinical Operations Manager - France

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Illkirch-Graffenstaden, Bas-Rhin, Grand Est, FRA
In-Office
Senior level
Healthtech
The Role
Manages clinical trial site contracting for complex studies, including budget grids, contract negotiations, investigator grants, regulatory documentation, and sponsor relationships. Oversees contracting performance, timelines, quality standards, and compliance while collaborating with sponsors, site activation teams, study teams, and quality management. Provides expert guidance, develops processes and training materials, presents to clients, and mentors colleagues.
Summary Generated by Built In

Job Title: Financial Clinical Operations Manager
Level: Manager
Location: France
 

Job Overview:
The Financial Clinical Operations Manager is responsible for managing contract strategies and supporting the delivery of start-up contracting activities for selected sponsors and complex studies or multi-protocol programs. This role includes the preparation negotiation and management of site agreements and preparing budget grids ensuring compliance with regulatory requirements and project goals. The Manager provides leadership in contracting processes collaborates with internal and external stakeholders and drives efficiency and quality in site activation activities.
 

IQVIA Overview:
IQVIA is a leading global provider of clinical research services commercial insights and healthcare intelligence to the life sciences and healthcare industries. Our work accelerates the development and commercialization of medical treatments that improve patient outcomes and population health worldwide. IQVIA’s global team of 88000+ professionals spans more than 100 countries supporting clinical research at every scale. As the world’s largest clinical trial site network and CRA footprint we empower our clinical teams to work confidently collaboratively and globally.
 

Responsibilities:

  • Preparing budget grids, estimates contracting strategies and coordination of grants to support proposal development.
  • Prepare and maintain contract templates budgeting systems processes and training materials tailored to selected sponsors and complex studies.
  • Oversee the preparation review negotiation and management of site regulatory documentation and clinical trial agreements with sponsors and sites.
  • Monitor contracting performance metrics ensuring compliance with project timelines financial targets and regulatory standards.
  • Collaborate with sponsors stakeholders and regional Site Activation (RSU) teams to successfully deliver project scopes in accordance with sponsor requirements and RSU Management Plans.
  • Provide expert legal operational and financial contracting support to study teams to facilitate efficient clinical trial initiation and maintenance.
  • Build strong long-standing relationships with preferred clients/customers ensuring satisfaction and alignment with organizational objectives.
  • Assess and review the contracting landscape to contribute insights and intelligence for assigned studies and broader organizational needs.
  • Ensure contracting efficiency and adherence to quality standards by implementing effective processes and systems.
  • Report on contracting performance metrics and identify out-of-scope activities implementing corrective actions when necessary.
  • Lead the development and review of technical scientific and administrative documentation to support study initiation and business development.
  • Work with Quality Management to maintain appropriate contract management and quality standards.
  • Mentor and coach colleagues delivering training materials and providing technical guidance for contracting processes.
  • Take a lead role in developing strategies to foster client engagement and build strong relationships with stakeholders.
  • Deliver presentations to clients and professional bodies to represent the organization’s expertise in contract management and site activation.
  • Serve as a liaison for non-specific projects with top clients/customers ensuring alignment with organizational goals and quality standards.

Qualifications:

  • Bachelor's Degree in Life Sciences or a related field.
  • 5-8 years of relevant sponsor or clinical research organization clinical site contracting experience including demonstrable experience acting as an international contract expert.
  • Extensive experience in site activation contract management and regulatory compliance.
  • Proven expertise in negotiating and managing clinical trial agreements and investigator grants.
  • Excellent communication and negotiation skills.
  • Ability to manage multiple projects and timelines effectively.
  • Proficiency in contracting systems and tools.

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

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Skills Required

  • Bachelor's degree in Life Sciences or a related field
  • 5-8 years of relevant sponsor or clinical research organization clinical site contracting experience
  • Demonstrable experience acting as an international contract expert
  • Extensive experience in site activation contract management and regulatory compliance
  • Expertise negotiating and managing clinical trial agreements and investigator grants
  • Excellent communication and negotiation skills
  • Ability to manage multiple projects and timelines effectively
  • Proficiency in contracting systems and tools

IQVIA Compensation & Benefits Highlights

The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about IQVIA and has not been reviewed or approved by IQVIA.

  • Healthcare Strength Healthcare coverage is positioned as comprehensive, spanning medical/dental/vision plus programs like telemedicine, EAP resources, and additional insurance options. Feedback suggests the health offering is a meaningful part of the overall rewards package, though details can vary by location and plan design.
  • Retirement Support Retirement benefits include an employer match structure that supports employee contributions through a defined formula. This adds steady long-term value to total rewards beyond base salary.
  • Leave & Time Off Breadth Time off offerings include vacation/paid time off, holidays, and flexibility themes, with some roles described as having discretionary or unlimited time-off models. This can make the package feel more attractive even when cash compensation is viewed as only mid-range.

IQVIA Insights

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The Company
HQ: Durham, NC
61,500 Employees
Year Founded: 2016

What We Do

IQVIA (NYSE:IQV) is a leading global provider of advanced analytics, technology solutions, and clinical research services to the life sciences industry. IQVIA creates intelligent connections across all aspects of healthcare through its analytics, transformative technology, big data resources and extensive domain expertise. IQVIA Connected Intelligence™ delivers powerful insights with speed and agility — enabling customers to accelerate the clinical development and commercialization of innovative medical treatments that improve healthcare outcomes for patients. With approximately 70,000 employees, IQVIA conducts operations in more than 100 countries. To learn more, visit www.iqvia.com.

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