Apprentice - Clinical Research

**Company Description**

AbbVie's mission is to discover and produce innovative medicines that provide solutions to the serious health problems of today while relevant to the medical challenges of tomorrow. We seek to transform people's lives in several key therapeutic areas such as immunology, oncology, neuroscience, opthamology, virology, in addition to relevant products and services from our Allergan Aesthetics portfolio. We are proud to be a** Great Place to Work company.**

AbbVie France is recruiting** 4 CRA (Clinical Research Associate) **as** apprentices. **The position is to be filled from **September 2024** for a period of **12 month **u nder the supervision of a qualified Clinical Research Associate (CRA). Our apprentices will conduct investigative site follow-up, solve study-related clinical site issues as they occur and initiate, recommend and communicate corrective action ensuring successful protocol level execution of Clinical Site Management deliverables involving start-up, execution and close-out of studies.

**Responsibilities**:_._
- Train to become knowledgeable of basic tasks in assigned area of responsibility. Demonstrates compliance with local regulations, Good Clinical Practices (GCPs), ICH Guidelines, AbbVie Standard Operating Procedures (SOPs), Monitoring Plans and to quality standards in conducting clinical research.
- Conduct all activities in a professional manner. Listen actively to acquire information and understand work procedures. Participate in the sharing of information to promote overall efficiency of the process. Attend and actively participate in meetings.
- Under supervision of a qualified CRA, help conducting on-site and off-site monitoring activities for Phase 1-4 studies to ensure successful execution of the protocol in accordance with applicable regulations, Good Clinical Practices (GCPs), ICH Guidelines, and AbbVie Standard Operating Procedures (SOPs) and business processes. Ensure all required documentation is available and valid in the Investigator Site File.
- Under supervision of a qualified person, help prepare documentation for regulatory submission dossier or perform any other activities related to start-up phase.
- Assist the qualified CRA in preparing site investigator payments as per executed contract obligations.
- Ensure Trial Master File completeness and accuracy, upload essential documents and perform Quality Control reviews of the documentation.
- Ensure completeness and accuracy of the data entered into the Clinical Trial Management System (LBE/actual date, Company personal, site staff ) or any other database as needed.

**Qualifications** Are you right for this role ?**
He or she should also be:

- rigorous, organized, proactive, and able to juggle multiple tasks
- curious, open-minded, adaptable and enjoy working in a team environment

What other information is important for you?

Working at AbbVie France also means benefiting from a work environment designed for its employees. O ur offices are located in the Rungis business park, 5 minutes from the city of Rungis, and served from Paris by the RER C, tram 7, and the 216 bus. A gym, as well as canteens, restaurants, and food trucks are also located in the business park.

Being an apprentice at AbbVie France means having the opportunity to be accompanied by a dynamic team that will help you develop your skills. It also means having your public transportation costs fully reimbursed, lunch vouchers and paid vacation.

Equality, diversity and inclusion are essential pillars for us. We are proud to have built an environment that allows each of our employees around the world to reach their full potential.

**Additional Information