NextRaiseNextRaiseFind jobs
Sign inSign up free
Jobs / Clinical Operations Manager in France
2 days ago
Apply with autofill
Apply with autofill
Iqvia·2 days ago
2 days ago

Financial Clinical Operations Manager - France

Illkirch, FranceMid · 5-10 yearsClinical Operations Manager

Sign up free to see how well your resume matches this role.

Boost your chances at iqvia

How you compare FREE

?
Your scoreYour score: not yet known
→
19
Top 10%Top 10%: 19 out of 100

Top 10% of NextRaise users, across all roles in this function in France.

Must-have skills for this role

  • contract management
  • site activation
  • clinical trial agreements
  • budgeting

PDF or DOCX · no account needed

Apply faster with autofill FREEThe NextRaise extension autofills your application in one click.careers.example.com/applyAutofillingFull namePriya SharmaEmailpriya.sharma@example.comPhone+49 30 1234567LocationBerlGet the extension

What you'll do

  • 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.

What they're looking for

  • 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.

Summarised by NextRaise from the employer’s description, which follows in full below.

Full description from employer

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.

Company

Iqvia
Illkirch, France

Company facts come from this company's own listings. We only show what the postings themselves carry.

Sourced from Iqvia's careers site·first seen 18 Sept 2026·last verified 18 Sept 2026·How we source jobs

Similar jobs

  • CADRE DE SANTE FORMATEUR (H/F) at fondationoeuvredelacroixsaintsimonParis, France–match not yet calculated
  • Product Expert - Clinical Operations at Veeva SystemsParis, France–match not yet calculated
  • Cadre de santé en Clinique SMR (H/F) at coliseefranceSaizy, France–match not yet calculated
  • Clinical Project Manager internship at sonioParis office, France–match not yet calculated
  • Coordinateur médical voltigeur - Worldwide (F/H) at medecins-du-mondeSaint, France–match not yet calculated

Browse more jobs

  • Clinical Operations Manager jobs in France
  • Clinical Operations Manager jobs in Germany
  • Clinical Operations Manager jobs in United States
  • Clinical Operations Manager jobs in Canada