Project Manager - Real World Evidence - France

IQVIA; Illkirch-Graffenstaden; Hybrid; EUR 60,000 - 90,000; Full time

Job summary

IQVIA in France seeks an experienced Clinical Project Manager to lead execution of clinical projects and support project teams. You will set up and maintain documentation, coordinate communications, and manage status and finance reports with cross‑functional teams.

The role requires 4–5 years of PM experience, knowledge of clinical trials and ICH GCP, and strong communication skills. Hybrid work with Paris or Bordeaux offices 2–3 times weekly is offered.

Qualifications

• Bachelor’s Degree Life sciences or related field Req.
• 4-5 years of prior relevant experience including > 1 years project management experience or equivalent combination of education, training and experience.
• Real World Evidence experience is valuable.
• Knowledge of clinical trials, regulatory requirements (ICH GCP) and guidelines relevant to clinical trials.
• Good communication and interpersonal skills.
• Hybrid role: needs to attend to Paris or Bordeaux offices 2-3 times per week.

Responsibilities

• Lead the execution of clinical projects and support project teams.
• Set up and maintain project documentation files and records.
• Lead with the creation and coordinate all information and communications for assigned projects.
• Update project plans, tracking systems and databases with project data.
• Prepare, analyze and distribute status, tracking and project finance reports.
• Coordinate project team and customer meetings via Web, telecon or face to face.
• Record minutes and follow up actions; coordinate with other project support staff.
• Serve as backup contact for internal project team as designated by study lead.

Skills

Project management

Communication

Time management

MS Office

Education

Bachelor’s Degree Life sciences or related field

Tools

MS Office

Job description

_ Job Overview _
Lead the execution of clinical projects and provide support to project teams related to the assigned project(s). Will support all project-related activities for assigned projects in accordance with SOPs, policies and practices.

_ _

_ Essential Functions _

• Establish new procedures and offer suggestions for process improvements for existing procedures.
• Set up and maintain all project documentation files and records.
• Proceed to investigators payment
• Lead with the creation and coordinate all information and communications for assigned projects.
• Update and maintain internal databases, tracking systems and project plans with project specific information.
• Prepare, analyze and distribute status, tracking and project finance reports.
• Prepare presentation materials for meetings and project summary data.
• Coordinate project team and customer meetings, identifying and planning appropriate medium (Web, telecon, face to face) and ensuring arrangements are handled appropriately.
• Determine and plan all meeting requirements in advance, as directed by the Project Manager.
• Take and record minutes, notes and actions at assigned meetings, distribute and follow up accordingly.
• Coordinate with other project support staff within and across the organization to identify and consolidate support processes.
• Will serve as backup contact for internal project team as designated by study lead.

_ Qualifications _

• Bachelor’s Degree Life sciences or related field Req
• 4-5 years of prior relevant experience including > 1 years project management experience or equivalent combination of education, training and experience
• Real World Evidence experience is valuable
• Knowledge of clinical trials - Knowledge of clinical trial conduct, and skill in applying applicable clinical research regulatory requirements i.e. ICH GCP and relevant local laws, regulations and guidelines, towards clinical trial conduct. Broad protocol knowledge; therapeutic knowledge desired. Good understanding of the competitive environment and how to communicate/demonstrate value through IQVIA solutions
• Good communication and interpersonal skills
• Good problem-solving skills
• Strong organizational skills
• Results and detail-oriented approach to work delivery and output
• Ability to work under close direction
• Strong software and computer skills, including MS Office application
• Ability to prioritize, actively seek input and problem solving
• Ability to work independently and manage time efficiently
• Ability to establish and maintain effective working relationships with coworkers, managers and clients
• Hybrid role: needs to attend to Paris or Bordeaux offices 2-3 times per week.

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.