Working in partnership with a single-sponsor.
Usually allocated to 1-2 protocols (likely to be in the areas of Oncology, Neurology, Immunology and/or Diabetes).
Responsible for approximately 10 sites.
On site between 6 and 8 days per month, dependent on the sponsor.
All CRAs and SCRAs are allocated a dedicated IQVIA Line Manager.
Permanent employment contract.
Sponsor model has reduced travel (approx. 30% or less) due to using the Risk Based Monitoring which incorporates remote monitoring therefore there is less need for on-site visits.

Have a degree in Life Sciences or have equivalent experience.
Have at least 1 or 2 years of independent on-site monitoring experience.
Be experienced in handling multiple protocols across a variety of drug indications with good time management skills.
Have a GCP knowledge.
Be flexible with the ability to travel nationwide.
Hold a full French and clean driving license.
Possess good communication, written and presentation skills are a must (must have fluency in English and French language).

Excellent salary and benefits package.
Flexible working hours in an office-based or a home-based role.
We invest in keeping our teams stable, so workload is consistent.
We offer genuine career development opportunities for those who want to grow as part of the organization.
We give the chance to work on cutting edge medicines, right at the forefront of new medicine development.

Junior Clinical Research Associate – Sponsor-dedicated

Key skills