Site Manager

il y a 1 jour

Paris, France Ergomed Temps plein

Company Description

Founded in 1997 by a Medical Doctor, Ergomed Plc is dedicated to the development of new drugs to save or improve lives. Operating with a global footprint in over 55 countries, Ergomed has the expertise to manage even the most challenging clinical trials. Ergomed provides services to over 100 clients in a range of therapy areas but excels in the provision of services for complex trials in Rare Diseases, Oncology and Neuroscience.

**Job Description**:

- Training, consultation and support of Study Site Coordinators /Research Nurses on clinical studies
- Providing non-operational site support to ensure progress of clinical study and to ensure that it is conducted, recorded, and reported in accordance with the protocol, standard operating procedures (SOPs), ICH GCP, and the applicable regulatory requirement(s)
- Notifying Study Monitor / Team on any site issues that are detected in contact with the clinical center and are relevant for them
- Establishing and maintaining relationships with Site Coordinators and Investigators to optimize performance of clinical study
- Assistance in development of recruitment strategies and tracking of recruitment or patient retention activities at the site

**Qualifications**:

- Bachelor or Master of Science degree or equivalent (preferably in medical field, i.e. medical nurse)
- Experience as a Clinical site manager, Study nurse or study site coordinator
- Excellent organisation skills with attention to detail
- Excellent interpersonal and communication skills
- Good IT skills (MS Word, Excel, Internet tools)

Additional Information

We offer excellent chances to progress and develop. We work on a global basis on interesting projects within rare diseases, oncology, and neurology. This is an ideal position to develop a career in clinical drug development.

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