Ucra

Labcorp is looking to hire an UNBLINDED CRA to monitor sites in Austria. You would be working within our Flexible Solutions department dedicated to one sponsor/client.

Would you like to work for one of the best known big pharma companies? Our sponsor is a global mid-sized pharma company with high working standards.

Are you passionate about growing in Clinical Field? We are proud to have an excellent team of the best professionals on the market and are looking for people who are ready to show true performance and interest in Clinical Trials.

Do you like responsibilities and challenges? As a Clinical Research Associate you will lead all aspects of study site monitoring according to Labcorp SOP, ICH guidelines and GCP. You will take part in pre-study qualification and initiation visits, routine monitoring, close-out of clinical sites, and maintenance of study files.
You will become a part of our team who is always ready to help. You will have a possibility to devote all your professional skills and knowledge into monitoring investigational sites as we organize our work environment and responsibilities with high standards.
Our sponsor invests heavily in training and crafts modern system of Clinical Trials so if you are passionate about working with a phenomenal team and expand your horizons feel free to reach us.

Education/Qualifications
- University or college degree, or certification in a related allied health profession from an appropriately accredited institution (e.g., nursing licensure);
- Ideally, you live in Vienna, Linz or Graz

Experience
- Ideally you have the ability to monitor study sites independently according to protocol monitoring guidelines, SOPs, GCP and ICH Guidelines
- You have excellent understanding of Serious Adverse Event (SAE) reporting
- Ability to resolve project-related problems and prioritize workload for self and team
- You have previous clinical research monitoring Experience (including pre-study, initiation, routine monitoring and closeout visits).
- Have native German and professional English language level

As a leading contract research organization (CRO), Labcorp Drug Development provides comprehensive drug development solutions for a range of industries. Our services cover the preclinical, clinical and post-market phases of drug development, the product life cycles for medical device and diagnostics and development services paired with regulatory support for the chemical testing and crop protection industries.

Labcorp Drug Development is a global leader in nonclinical safety assessment, clinical trial testing and clinical trial management services. Our unique perspectives are based on decades of scientific, medical and regulatory expertise.

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