# Clinical Project Coordinator

**Company**: IQVIA
**Work arrangement**: hybrid
**Experience**: mid
**Job type**: full-time
**Category**: Healthcare
**Industry**: Healthcare

**Apply**: https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Illkirch-Graffenstaden-France/Project-Manager---Real-World-Evidence_R1575687?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply
**Canonical**: https://yubhub.co/jobs/job_74e5d3fe-6eb

## 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

### Required
- Life Sciences
- Project Management
- Clinical Trials
- ICH GCP
- MS Office

### Nice to have
- Real World Evidence

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Source: [Apply at iqvia.wd1.myworkdayjobs.com](https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Illkirch-Graffenstaden-France/Project-Manager---Real-World-Evidence_R1575687?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply)