Clinical Research Associate

il y a 5 jours


Paris, France Scope International France Temps plein

Prise de poste : 03/03/2025 BAC +5 Paris

Nombre de poste : 1 CDI Rémunération non définie

**Description du poste et des missions**:
**SCOPE International** is an independent Full-Service Contract Research Organization (CRO) with a network of 15 local offices and business entities throughout Europe and USA. SCOPE offers a complete range of clinical development and consulting services to the pharmaceutical, biotechnology and medical device industries, and is supported by long established partnerships in other geographies.

**Scope International France** has an exciting opportunity for a Clinical Research Associate (CRA) with 1 ½ -2 years on-site monitoring experience to take the next step in their career and join our growing FR team.

**Profil souhaité**:
**You will**:

- Preparation and submit the regulatory files.
- Perform clinical trial site evaluation, initiation, routine monitoring and close out visits.
- Review and ensure Investigator Site Files (ISFs) are up to date and collect essential documents for the Trial Master File (TMF)
- Ensure proper handling, accountability and reconciliation of all Investigational Product(s) and clinical trial supplies.
- Update all relevant tracking systems on an ongoing basis.
- Prepare and submit trip reports according to project timelines.

Interact directly with sites, including clinical investigators and other health care professionals involved in the clinical trial to maintain a positive rapport and ensure project expectations are met.

**Compétences requises**:
**Qualifications & Requirements**:

- A Master or higher graduate degree within a science related field, with a CRA training.
- 1-2 years of on-site monitoring experience required.
- Ability and willingness to travel up to 80%, depending on project needs.
- Competent in written and oral English and French (German would be one more)
- Excellent organization and communication skills.
- Ability to prioritize multiple tasks and achieve project timelines.
- Ability to take initiative and work autonomously.
- Computer skills (Microsoft Office).



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