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CRA 1 and 2 for Sponsor Specific - Austria

Aplica ya
Mapa de ubicación: Vienna, Austria Full time R1211032

Descripción del trabajo

We are looking to recruit committed individuals to work in a busy clinical research department providing essential monitoring support.The role provides the opportunity to develop monitoring skills with advanced responsibilities, critical and central to the conduct of the clinical project.The CRA oversees the progress of a Clinical Trial, ensuring that it is conducted, recorded and reported in accordance with the protocol, Standard Operating Procedures (SOPs), Good Clinical Practice (GCP) and the applicable Regulatory requirements

What we Offer:

  • Excellent salary and benefits package

  • Company car or car allowance

  • Depending on the model, home-based is a possibility

  • Flexible working hours in a home-based role

  • As a CRA, you will receive a company iPad and have use of key developments such as site visit apps, visit reporting apps which allow CRAs to do their day to day job more efficiently!

  • 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

  • On site between 6 and 9 days per month, dependent on the sponsor

  • All CRAs and SCRAs are allocated a dedicated IQVIA Line Manager

  • Permanent employment contract

  • Fantastic work/life balance - flexible working within the core hours of 10 am to 4 pm

  • Sponsor model has reduced travel (approx. 30% or less) due to using ‘Fit for Purpose Monitoring’ which incorporates remote monitoring therefore there is less need for on-site visits

Responsibilities:

  • Site management and monitoring activities across the Turkey

  • 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

  • Have at least 2 years of independent on-site monitoring experience

  • Be experience 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 local and clean driving license

  • Possess strong communication, written and presentation skills are a must (must have fluency in English language

Become part of our team.

Whatever your career goals, we are here to ensure you get there!

We invite you to join IQVIA™.

At IQVIA, we believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world. The advanced analytics, technology solutions and contract research services we provide to the life sciences industry are made possible by our 70,000+ employees around the world who apply their insight, curiosity and intellectual courage every step of the way. Learn more at jobs.iqvia.com.

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