2 beste Stellen als “clinical trial coordinator “ in münchen – aktuell auf Personalsuche

Clinical Research Associate I in Germany or in Austria
Fortrea —München
- Vollzeit
- Nursing
- Management-Erfahrung
- Mit Reiseanteil
13 Tage
Site Engagement Leader (m/f/d)
GlaxoSmithKline —München
- 85.500 € – 142.500 € pro Jahr
- Vollzeit
- Ohne Hochschulabschluss

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Clinical Research Associate I in Germany or in Austria

Fortrea -
München

Jetzt bewerben

Details zur Stelle

Vollzeit
vor 13 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 trial coordinator “ Jobs in münchen

Clinical Research Associate I in Germany or in Austria

Site Engagement Leader (m/f/d)

Ich möchte aktuelle Job-E-Mails für Stellen als “clinical trial coordinator “ 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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