Job Overview:
Trainee CRA/ Junior CRA

Become a CRA with Covance Paris

You know how difficult it is to become CRA without experience, it can be frustrating.

Covance France have created a development path so that professionals with little Clinical Research experience can develop the profession from the ground up, starting from the basics to independent monitoring, working on real, life changing clinical trials.

This path requires commitment, since depending on previous experience it may take a minimum of 2 years from the start of the path to become an independent CRA. If this is fine with you, t hese jobs would suit professionals who:

• Live in Paris , and are keen to work based from our offices for the whole development period.
• Bring min 6 monthsexperience in a related clinical trial field (study coordinator, study nurse, Clinical Trial Assistant, Pharmacovigilance, Data Management, etc.)
• Have completed a University/ College degree in Life Sciences or a certification from an appropriately accredited Health institution, mainly nursing)

With these jobs you will grow, among other, your skills:

• Building constructive relationships with investigative sites, and ensuring subjects are complying with protocol requirements, study visits, and timelines.
• Monitoring site performance and implementing action plans for sites not meeting expectations, in conjunction with the CRA
• Assisting CRAs with preparation for site visits (i.e. running reports, QC of files (checking for missing documents), resolving action items from previous visits).
• Performing Case Report Form review, query generation and resolution against established data review guidelines.

You will accompany more experienced CRAs to all types of site visits until gradually you are entitled to perform them autonomously

The work we do at Covance impact the lives of millions of people around the world... so could you too as our future CRA!
Education/Qualifications:

• University/college degree in one of the life sciences
• Ideal: CRA training program

Experience:
Minimum Required:

• Bring min 6 monthsexperience in a related clinical trial field (study coordinator, study nurse, Clinical Trial Assistant, Pharmacovigilance, Data Management, etc.)
• Basic understanding of biology and biological processes
• Good organizational and time management skills
• Good communication skills, oral and written
• Exhibit general computer literacy
• Works efficiently and effectively in a matrix environment