Rwe Project Manager

il y a 5 jours

Paris, France Excelya Temps plein

Created in 2014, Excelya is a people-centered Contract Research Organization (CRO) that excels with care.

We offer a personal and authentic experience within a young, ambitious health company on the path to becoming the clinical research leader in Europe thanks to our 800 Excelyates. Our unique one-stop provider service model - leveraging full-service, functional service provider and consulting - allows our Excelyates to evolve through a diverse array of projects. In collaboration with preeminent experts, Excelya advances scientific, managerial and human knowledge to improve the patient journey.

For our team members, excelling with care means benefitting from a stimulating professional environment that encourages personal, intellectual, and operational participation so that together we can be the best in our field. We commit to giving each Excelyate the means to express their natural talents, develop their full potential and invest their unique selves in our unique project.

**What we offer**:
As a member of the Oncology Medical Department, your role will be to design, set up and monitor real-life studies. These studies may respond to internal needs (preparation of transparency files, setting up international studies, assessing the impact of our products) or to the external needs of health authorities (post-registration studies), striving as far as possible to anticipate them, by making proposals to the Authorities upstream.
- Drafting of study protocols
- Monitoring the activities of service providers
- Analysis and publication of results.

**Minimum Requirements**:

- Basic scientific training (minimum 5 years’ higher education)
- Experience in project management
- Significant experience in epidemiology in the pharmaceutical industry (Medical Affairs, Clinical Research, Epidemiology, Pharmacoeconomics, etc.), in an academic environment or in a public health or private research organization (epidemiology, RWE, etc.).
- You demonstrate initiative, analytical skills and scientific rigor.
- You enjoy working as part of a team and helping others to progress by sharing your skills.
- You have a good knowledge of clinical trials and data management.
- Good command of IT tools (Pack Office) and statistical software (SPSS, SAS, other).
- Fluency in English is required.

**Summary**:

- Type of job:
Full-time
- Location:
Paris Area
- Capability:
Clinical Research

**Contact**:

- **Clara Rousselet-Blanc**
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