1 beste Stelle als clinical research associate study nurse in münchen – aktuell auf Personalsuche

Clinical Research Associate I in Germany or in Austria
Fortrea —München
- Vollzeit
- Nursing
- Management-Erfahrung
- Mit Reiseanteil
14 Tage

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Clinical Research Associate I in Germany or in Austria
Fortrea —München
Contribute to study progress by helping sites meet recruitment, quality, and timeline objectives. At Fortrea, we welcome ambitious clinical research…
14 Tage

Ich möchte aktuelle Job-E-Mails für Stellen als clinical research associate study nurse in münchen erhalten

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Clinical Research Associate I in Germany or in Austria

Fortrea -
München

Jetzt bewerben

Details zur Stelle

Vollzeit
vor 14 Tagen

Qualifikationen

Nursing
Management-Erfahrung
Pharmazie

Vollständige Stellenbeschreibung

Are you ready to take the next step in your clinical research career and transition into a Clinical Research Associate role?

We are looking for motivated professionals with experience as a Study Nurse, Study Coordinator, Clinical Trial Assistant (CTA), or In-House CRA who are eager to move into onsite monitoring and build a successful CRA career.

You will contribute to the execution of clinical studies across a variety of therapeutic areas, including Oncology, Dermatology, Respiratory, Cardiology, and Diabetes, gaining broad exposure and hands‑on experience while developing your monitoring skills.

Key Responsibilities:

Support the management of clinical trial sites in compliance with ICH-GCP, study protocols, sponsor requirements, and Fortrea SOPs.
Participate in site initiation, routine monitoring, and close-out visits under the guidance of experienced CRA colleagues.
Conduct source data verification (SDV) and support data review activities to ensure data quality and patient safety.
Assist sites with study-related questions and support issue resolution in collaboration with cross-functional teams.
Maintain clinical trial documentation and support eTMF completeness and inspection readiness.
Contribute to study progress by helping sites meet recruitment, quality, and timeline objectives.

Required Qualifications:

Degree in Life Sciences, Nursing, Pharmacy, or a related scientific discipline.
Experience in clinical research as a Study Nurse, Study Coordinator, CTA, Clinical Trial Associate, In-House CRA, or similar role.
Good understanding of clinical trial processes and ICH-GCP guidelines.
Strong organizational skills, attention to detail, and a proactive mindset.
Fluent in German and English, both written and spoken.
Willingness to travel for onsite monitoring visits across Germany.

Why Join Us?

Grow your clinical research career in a structured and supportive environment with clear development pathways and mentoring.
Gain hands‑on exposure to global clinical trials and multiple therapeutic areas while building strong foundational CRA skills.
Benefit from formal training programs, modern clinical systems, and continuous learning opportunities.
Enjoy a flexible work model, competitive benefits, and a culture that values collaboration, quality, and well‑being.

At Fortrea, we welcome ambitious clinical research professionals who are ready to make the move into monitoring. If you have experience supporting clinical trials and are looking for your first CRA opportunity, we'd love to hear from you.

Learn more about our EEO & Accommodations request here .

Jetzt bewerben

Erweiterte Suche

clinical research associate study nurse Jobs in münchen

Clinical Research Associate I in Germany or in Austria

Related jobs to explore

Ich möchte aktuelle Job-E-Mails für Stellen als clinical research associate study nurse in münchen erhalten

Weitere Job-Standorte erkunden

Are you ready to take the next step in your clinical research career and transition into a Clinical Research Associate role?

We are looking for motivated professionals with experience as a Study Nurse, Study Coordinator, Clinical Trial Assistant (CTA), or In-House CRA who are eager to move into onsite monitoring and build a successful CRA career.

You will contribute to the execution of clinical studies across a variety of therapeutic areas, including Oncology, Dermatology, Respiratory, Cardiology, and Diabetes, gaining broad exposure and hands‑on experience while developing your monitoring skills.

Key Responsibilities:

Support the management of clinical trial sites in compliance with ICH-GCP, study protocols, sponsor requirements, and Fortrea SOPs.

Participate in site initiation, routine monitoring, and close-out visits under the guidance of experienced CRA colleagues.

Conduct source data verification (SDV) and support data review activities to ensure data quality and patient safety.

Assist sites with study-related questions and support issue resolution in collaboration with cross-functional teams.

Maintain clinical trial documentation and support eTMF completeness and inspection readiness.

Contribute to study progress by helping sites meet recruitment, quality, and timeline objectives.

Required Qualifications:

Degree in Life Sciences, Nursing, Pharmacy, or a related scientific discipline.

Experience in clinical research as a Study Nurse, Study Coordinator, CTA, Clinical Trial Associate, In-House CRA, or similar role.

Good understanding of clinical trial processes and ICH-GCP guidelines.

Strong organizational skills, attention to detail, and a proactive mindset.

Fluent in German and English, both written and spoken.

Willingness to travel for onsite monitoring visits across Germany.

Why Join Us?

Grow your clinical research career in a structured and supportive environment with clear development pathways and mentoring.

Gain hands‑on exposure to global clinical trials and multiple therapeutic areas while building strong foundational CRA skills.

Benefit from formal training programs, modern clinical systems, and continuous learning opportunities.

Enjoy a flexible work model, competitive benefits, and a culture that values collaboration, quality, and well‑being.

At Fortrea, we welcome ambitious clinical research professionals who are ready to make the move into monitoring. If you have experience supporting clinical trials and are looking for your first CRA opportunity, we'd love to hear from you.

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