Sponsor Dedicated DACH Clinical Research Associate based in Germany

FTGER Fortrea Germany GmbH; München; Remoto; EUR 60.000 - 90.000; Tempo pieno

Descrizione del lavoro

Fortrea Germany GmbH is seeking a Clinical Research Associate to monitor sites in Austria and Switzerland, supporting sponsor-dedicated studies with high impact on patient care.

You will conduct pre-study, initiation, monitoring and close-out visits, ensure data quality and protocol compliance, build strong site relationships, and coordinate regulatory activities across regions.

Competenze

• University or college degree in life sciences, nursing, pharmacy, or a related allied health profession; equivalent relevant experience may be considered in lieu of formal education.
• Basic to good knowledge of ICH/GCP Guidelines and applicable local laws and regulations governing clinical trials.
• Solid understanding of clinical research processes, regulations, and methodology.
• Strong organizational and time management skills.
• Ability to build and maintain relationships.
• 1 to 3 years of monitoring experience required within CRO or Pharma environment.

Mansioni

• Identify and assess new potential investigators and sites.
• Recommend sites during feasibility and selection phases.
• Conduct pre-study, initiation, monitoring, and close-out visits.
• Monitor site performance, data quality, and protocol compliance.
• Act as a key point of contact for site personnel, providing training and support.
• Use data insights to assess risks and drive decisions.
• Support regulatory audits, EC submissions, and system access coordination.

Conoscenze

Monitoring

ICH-GCP knowledge

Regulatory compliance

Time management

Relationship building

Formazione

Life sciences degree or equivalent

Descrizione del lavoro

Make a meaningful impact in clinical research by joining our sponsor-dedicated team as a Clinical Research Associate (CRA). This role offers the opportunity to monitor sites in Austria and in Switzerland, while working on cutting-edge studies that shape the future of healthcare. #LI-GQ1 #LI-Remote

Key Responsibilities

• Identify and assess new potential investigators and sites.
• Recommend sites during feasibility and selection phases.
• Conduct pre-study, initiation, monitoring, and close-out visits.
• Monitor site performance, data quality, and protocol compliance.
• Act as a key point of contact for site personnel, providing training and support.
• Use data insights to assess risks and drive decisions.
• Support regulatory audits, EC submissions, and system access coordination.

Required Qualifications

• University or college degree in life sciences, nursing, pharmacy, or a related allied health profession; equivalent relevant experience may be considered in lieu of formal education.
• Basic to good knowledge of ICH/GCP Guidelines and applicable local laws and regulations governing clinical trials.
• Solid understanding of clinical research processes, regulations, and methodology.
• Strong organizational and time management skills.
• Ability to build and maintain relationships.
• 1 to 3 years of monitoring experience required within CRO or Pharma environment.

Why Join Us?

• Be part of a sponsor-dedicated team with a strong pipeline and purpose.
• Enjoy regional monitoring-minimizing travel while maximizing your impact.
• Collaborate with passionate professionals in a supportive environment.
• Contribute to meaningful research that improves lives.

At Fortrea, we're all about turning the "impossible" into "I'm possible." Together, we break barriers to deliver exceptional service to our patients, fueled by a shared commitment to teamwork and excellence. Regardless of your role, we're all family, working together to achieve extraordinary results. At Fortrea, your career isn't just a job - it's a journey of making the exceptional possible, every day.