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From the employer's careers site First seen 27 Oct 2026

Clinical Project Coordinator

IQVIA Hybrid mid full-time

The employer hasn't listed a salary.

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Description

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

Responsibilities

  • Establish new procedures and offer suggestions for process improvements for existing procedures.
  • Set up and maintain all project documentation files and records.
  • Coordinate investigator payments.
  • Lead the creation and coordination of 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.
  • Serve as backup contact for internal project team as designated by study lead.

Requirements

  • Bachelor's degree in Life Sciences or related field.
  • 4-5 years of prior relevant experience, including > 1 year of project management experience or equivalent combination of education, training and experience.
  • Real World Evidence experience is valuable.
  • Knowledge of clinical trials, including clinical trial conduct, and skill in applying applicable clinical research regulatory requirements (e.g. ICH GCP and relevant local laws, regulations and guidelines).
  • 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 applications.
  • Ability to prioritize, actively seek input and problem-solve.
  • 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.

Skills

Nice to have

  • Real World Evidence

Ready to apply?

You apply with the employer directly. Their original posting is here: https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Illkirch-Graffenstaden-France/Project-Manager---Real-World-Evidence_R1575687

Apply on IQVIA