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Tech Stack
Tools & technologiesGoogle Cloud Platform
About the role
Key responsibilities & impact- 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.
Requirements
What you’ll need- 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).
Benefits
Comp & perks- 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.
ATS Keywords
✓ Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills & Tools
GCP knowledgeindependent on-site monitoring experiencehandling multiple protocolstime management
Soft Skills
communication skillswritten skillspresentation skillsflexibility
