Offres d'emploi

Le poste

Clinical Project Coordinator - Entry Level

 

Due to continuous business growth and a strong study pipeline, we are currently looking to hire Project Coordinators to join our successful and growing France team and engage in clinical trial management on a day-to-day level. This position will work with our operational teams to accomplish tasks and projects that are instrumental to the company's success. This position will provide extensive training and is suitable for recent graduates; internship, industrial placement, Clinical Trials experience is also beneficial.

Responsibilities: 

• Work closely with the Project Clinical Trial Manager for timely delivery of recurrent tasks consistently with a high degree of accuracy;
• Compile and maintain project-specific status reports within the Clinical Trial Management System (CTMS);
• Interact with the internal project team, Sponsor, study sites, and third-party vendors;
• Ownership of the Trial Master File;
• Create and maintain project timelines and enrollment projections; and
• Coordinate project meetings and produce quality minutes.

Qualifications:

• Bachelors' Degree in Life Sciences, Master's Degree preferred;
• Excellent oral and written English & French Languages ​​communication skills;
• Knowledge of Microsoft Office programs;
• Experience in a health sciences or business setting preferred;
• Excellent organizational and prioritization skills;
• Strong attention to detail.

We kindly request applicants to submit their CV in English.

 

Please apply via the link provided to our careers site. 

 

Voir l'annonce sur le site de l'entreprise

 

 

L'entreprise

Medpace

 

Medpace is a global Clinical Research Organisation (CRO) partnering with leading pharmaceutical, biotech, and device companies to bring promising new drugs and devices to market. Medpace combines efficient clinical trial management with comprehensive regulatory consulting to provide clients with exceptional support during the drug development process. We manage the full drug and device development process for our clients which includes many components: clinical development plan preparation, project management, regulatory document preparation, safety surveillance, clinical monitoring, data management, statistical analysis, medical writing, quality assurance auditing, and regulatory submissions.

Employing almost 6,000 people across 40+ countries, our people are our biggest asset and embody our values and our approach to serving our clients. They work hard, understand our high expectations, and rise to the challenge. In return, they are rewarded with interesting projects, career advancement, and recognition. Whether you are a recent graduate or seasoned in your field, your contributions can make an impact on our business.