Clinical Research Associate (no travel)

IQVIA

  • Amsterdam, Noord-Holland
  • Vast
  • Voltijds
  • 6 uren geleden
IQVIA™ is the leading human data science company focused on helping healthcare clients find unparalleled insights and better solutions for patients. Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness the power of healthcare data, domain expertise, transformative technology, and advanced analytics to drive healthcare forward.Clinical FSP BusinessIQVIA clinical FSP business is unique. Our teams are dedicated to a single sponsor partner, where the common goal is quality delivery for our clients. We set ourselves apart with collaboration and face to face contact both at start up and during the clinical study.We are recognised as one of the most admired companies in the world to work for by Fortune magazine. The reason we have continually received this accolade is our commitment to continued growth and development.We understand that everyone looks for new opportunities for different reasons, within our Dutch team we aim to make sure you have a job you are happy with and not just a job. Are you looking for a role with reduced travel, a homebased role, continued training, locally based manager, and a structured career path? We will work with you during the recruitment process to understand what is important to you.What we Offer:
  • Excellent salary and benefits package
  • Company car or car allowance
  • Flexible working hours in 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 organisation
  • 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
  • No site visits with no travel
  • All CRAs and SCRAs are allocated a dedicated IQVIA Line Manager
  • Fantastic work/life balance
Responsibilities:
  • Site management and monitoring activities across the country
  • 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
To become part of our team, you should:
  • Have a degree in Life Sciences or have equivalent experience within a nursing background.
  • Have at least 18 months of independent on-site monitoring experience
  • 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 full and clean driving license
  • Possess strong communication, written and presentation skills are a must (must have fluency in English and Dutch language)
  • Whatever your career goals, we are here to ensure you get there!
We invite you to join IQVIA™.Join UsMaking a positive impact on human health takes insight, curiosity, and intellectual courage. It takes brave minds, pushing the boundaries to transform healthcare. Regardless of your role, you will have the opportunity to play an important part in helping our clients drive healthcare forward and ultimately improve outcomes for patients.Forge a career with greater purpose, make an impact, and never stop learning.#CRASDAJDIQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at

IQVIA