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Single Sponsor- experienced CRA - Denmark

IQVIA Clinical Functional Services Partnerships (FSP) business is unique. Our teams are dedicated to a single sponsor partner, where the common goal is quality delivery for our customers. We set ourselves apart with collaboration and face to face contact both at start up and during the clinical study.

Leadership recognises the skills, talent and experience of our clinical teams and strives to build upon this as the function evolves and grows. Our managers understand the sponsors priorities and the individual aspects of each model. Focus is given to career development from day one, including new hire orientation and onboarding, day to day problem solving and training and development.

Unique to the FSP model, our team contributes to the pipelines of the specific sponsor and therefore our CRAs are ‘indication and molecule experts’. Additionally, IQVIA’s FSP business works with the Sponsors SOP’s, creating more continuity for both parties.

Our models offer excellent opportunities for experienced CRA’s to expand their knowledge and skills.

What we Offer:

  • Excellent salary and benefits package
  • Flexible working hours in an office-based or a home-based role anywhere in Denmark
  • 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
  • Role Details:

  • Working in partnership with a single-sponsor
  • Usually allocated to 2-3 protocols (likely to be in the areas of Oncology, Neurology, Immunology and/or Diabetes)
  • Responsible for approximately 15 sites
  • On site between 6 and 9 days per month, dependant on the sponsor
  • All CRAs and SCRAs are allocated a dedicated IQVIA Line Manager
  • Permanent employment contract
  • Sponsor model might have reduced travel (approx. 30% or less) due to using ‘Fit for Purpose Monitoring’ which incorporates remote monitoring therefore there might be less need for on-site visits
  • Responsibilities:

  • Site management and monitoring activities across Denmark
  • Work with sites to adapt, drive and track subject recruitment plan
  • Provide protocol and study training to the assigned sites
  • Create and maintain monitoring visit reports and action plans
  • If appropriate, co-monitor, train and mentor junior members of the team
  • Become part of our team.

    We believe in hiring the best talent in the industry.

    To become part of our team, you should:

  • Have at least 2 years of independent on-site monitoring experience
  • Have a degree in Life Sciences or have equivalent experience with a nursing background.
  • Be experienced in handling multiple protocols across a variety of drug indications with good time management skills
  • Have in depth GCP knowledge
  • Be flexible with the ability to travel nationwide
  • Hold a clean driving license
  • Possess strong communication, written and presentation skills are a must (must have fluency in Danish and English languages)
  • Whatever your career goals, we are here to ensure you get there!
  • We invite you to join IQVIA™.


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