Clinical Research Associate Sponsor Dedicated in Austria

Fortrea; Österreich; Hybrid; EUR 50 000 - 70 000; Vollzeit

Zusammenfassung

Fortrea, a leader in the CRO field, seeks a Sponsor-Dedicated CRA to oversee clinical trials in the Medical Device/Diabetes sector. The role involves monitoring compliance, ensuring patient safety, and collaborating closely with sponsors. Candidates should possess a relevant degree, understanding of GCP, and be fluent in both German and English. Fortrea offers a flexible, supportive work environment focused on career growth.

Leistungen

Competitive salary and performance bonuses

Flexible work arrangements (hybrid/remote options)

Career growth environment

Opportunity to work on innovative studies with leading sponsor

Qualifikationen

• University or college degree or certification in a related allied health profession.
• Strong understanding of GCP guidelines and monitoring procedures.
• Basic understanding of the clinical trial process.

Aufgaben

• Monitor clinical trial sites for compliance with protocols and regulations.
• Build relationships with investigators and ensure high-quality data collection.
• Perform on-site monitoring visits.

Kenntnisse

Fluent in German

Fluent in English

Understanding of ICH GCP Guidelines

Understanding of clinical trial process

Ausbildung

University or college degree in a related field

Jobbeschreibung

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 is your chance!

Key Responsibilities:

In this role, you will

• 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
  

Qualifications:

• University or college degree, or certification in a related allied health profession from an appropriately accredited institution (Fortrea may consider relevant and equivalent experience in lieu of educational requirements)
  
• Thorough understanding of ICH GCP Guidelines, of local regulatory requirements and of monitoring procedures.
  
• Basic understanding of the clinical trial process.
  
• Fluent in German and in English, both written and verbal.
  

What We Offer:

• Competitive salary and performance bonuses
  
• Flexible work arrangements (hybrid /remote options)
  
• Career growth environment in a supportive environment
  
• Works directly with a leading sponsor on innovative studies
  

Ready to take your CRA career to the next level? Apply now!

#LI-GQ1 #LI-Remote

Fortrea is actively seeking motivated problem-solvers and creative thinkers who share our passion for overcoming barriers in clinical trials. Our unwavering commitment is to revolutionize the development process, ensuring the swift delivery of life-changing ideas and therapies to patients in need. Join our exceptional team and embrace a collaborative workspace where personal growth is nurtured, enabling you to make a meaningful global impact. For more information about Fortrea, visit www.fortrea.com.

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.

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