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Salary
$50k – $86k per year (Estimated)
Location
In office (France)
Seniority
Senior · 5+ years exp
Employment
Full-Time
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IQVIA is an American company formed in 2016 by the merger of the contract research organisation Quintiles, founded in 1982, with the pharmaceutical data business IMS Health. It runs clinical trials on behalf of drug and device makers and simultaneously operates one of the largest healthcare data estates in the world, covering prescriptions, claims and electronic medical records, which it sells back to the same industry for commercial planning and real-world evidence studies. Headquartered in Durham, North Carolina and listed on the New York Stock Exchange, it employs close to ninety thousand people and combines the trial and data businesses in what it calls connected intelligence.

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 preparingbudget gridsensuring 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.

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