Apex Clinical Research Associate- France

Join theAPEX CRA Program in France!
Are you a recent graduate and do you have 1 year or less of clinical experience?Did you study in the life sciences/data sciences/data analytics/clinical/nursing area?
The Accelerated Program of Education, Exposure, and Experience for CRAs(APEX CRA)provides foundational Clinical Research training-including project and system experience-to new CRA hires who are recent college graduates and have less than a year of monitoring experience.
Through this program, you'll transform into a credible and experienced CRA I.As you progress, APEX CRAs perform billable project tasks to support the CRAs and Clinical Operations Leads (COLs)witha focus inthree developmental areas: Project Support, Initiation CRA support, and Site Facing support. You'll be required to complete the ACRP Entry Level Knowledge Assessment and are enrolled in a 1-year membership to the ACRP. You'll also work closely with CRAs to gain exposure to and experience with the CRA role and its responsibilities across a period of three to six months.
During this experience, you'll have the opportunity to practically apply in-class concepts with day-to-day application byworkingwithclinical systems including Clinical Trial Management Systems (CTMS), Electronic Data Capture, Safety Information Systems, and TMF platforms, and benefit from both instructor-ledtrainings and ongoing coaching and support of Line Managers andCOLs. Finally, APEX CRAs accompany CRAs for observational and co-monitoring support on-site or during remote visitswhich combines learningfor the APEX CRAs and workloadaidfor theirCRAcolleagues.Upon completion of the program, you're well-positioned to independently function within the CRA role and to immediately begin successful monitoring! More about you
Please note* You must have the right to live and work in France without Sponsorship with an April start date.
Requirements:

• Bachelor’s or equivalent degree in biological science, pharmacy or other health related discipline.
  
• Fluent in French
  
• Strong interpersonal, written, and verbal communication skills within a matrixed team.
  
• Experience working in a self-driven capacity, with a sense of urgency and limited oversight.
  
• A client-focused approach to work and flexible attitude with respect to assignments/new learning.
  
• The ability to manage multiple tasks, evaluate a variety of unpredictable scenarios and achieve project timelines while being able to apply your understanding of study protocol(s).An honest and ethical work approach to promote the development of life changing treatments for patients.
  
• Strong computer skills, including but not limited to the knowledge of a Clinical Trial Management System (CTMS), Electronic Document Management System (EDMS) and MS-Office products such as Excel and Word.