Clinical Research Associate

vor 1 Woche

Wien, Österreich Fortrea Vollzeit

As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access, and technology solutions across more than 20 therapeutic areas. Conducting operations in ~100 countries, Fortrea is transforming drug and device development for partners and patients across the globe.

As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access, and technology solutions across more than 20 therapeutic areas. Conducting operations in ~100 countries, Fortrea is transforming drug and device development for partners and patients across the globe.

We are seeking a **Sponsor-Dedicated CRA** with solid monitoring experience to be part of a **clinical trial in Medical Device/Diabetes**. If you are eager to make an impact, this you chance

**Responsibilities**:

- Monitor clinical trial sites to ensure compliance with protocols, GCP, and regulatory requirements
- Build strong relationships with investigators and site staff
- Ensure high-quality data collection and patient safety
- Work closely with the sponsor, providing insights and updates on study progress
- Perform on-site monitoring visits in Austria
- ** Qualifications**:

- University or college degree, or certification in a related allied health profession from an appropriately accredited institution (e.g., nursing licensure). An equivalent amount of experience can be substituted as appropriate.
- Thorough understanding of ICH GCP Guidelines and understanding of local regulatory requirements. - Thorough knowledge of monitoring procedures.
- Basic understanding of the clinical trial process.
- Fluent in German and in English, both written and verbal.
- _ Fortrea may consider relevant and equivalent experience in lieu of educational requirements_.

**Experience**:

- A minimum of 2 years of Clinical Monitoring experience.
- Ability to monitor study sites independently according to monitoring plan, project requirements, SOPs, and ICH GCP guidelines.
- Ability to work with mínimal supervision.
- Have an understanding of the Serious Adverse Event (SAE) reporting, process production of reports, narratives and follow up of SAEs.
- Good planning, organization, and problem-solving abilities.
- Works efficiently and effectively in a matrix environment.

**Why Join Us?**
- Works directly with a leading sponsor on innovative studies
- Career growth environment in a supportive environment

LI-GQ1

**Fortrea is proud to be an Equal Opportunity Employer**:
As an EOE/AA employer, Fortrea strives for diversity and inclusion in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications of the individual and do not discriminate based upon race, religion, color, national origin, gender (including pregnancy or other medical conditions/needs), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. We encourage all to apply.

For more information about how we collect and store your personal data, please see our Privacy Statement.

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