CRA 1 and 2 for Sponsor Specific - Austria
Vienna, Austria
vor 4 Tg.

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™.

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