CRA 1 and 2 for Sponsor Specific - Austria
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
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
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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