20 beste Stellen als study nurse in bayern – aktuell auf Personalsuche

Clinical Research Associate I in Germany or in Austria
Fortrea —München
- Vollzeit
- Nursing
- Management-Erfahrung
- Mit Reiseanteil
13 Tage
Study Nurse (m/w/d)
Invisio Clinical Studies Consulting GmbH —Nürnberg
- Teilzeit
- Englisch
- Microsoft Office
- Mit Reiseanteil
Studienkoordinator/Study Nurse
Barmherzige Brüder —München
- Teilzeit
- Krankenhaus
- Patientenbehandlung
- Dateneingabe
- Mitarbeiter-Rabatt
- Weiterbildungsprogramme
Study Nurse (m/w/d)
Deutsches Herzzentrum München TUM Universitätsklinikum —München
- Vollzeit
- Patientenbehandlung
- Dateneingabe
Medizinische/-r Studienassistent/-in, Wecare (m/w/d)
Klinik St. Hedwig —Regensburg
- Online-Bewerbung
- Krankenhaus
- Patientenbehandlung
- Recruiting
- Weiterbildungsprogramme
Study Nurse (m/w/d)
LMU Klinikum München —München
- Vollzeit
- Blutentnahme
- Doktorat
- Master
- Weiterbildungsprogramme
- Flexible Arbeitszeiten
12 Tage
Study Nurse (Teilzeit 50-60%) (m/w/d)
LMU Klinikum München —München
- Teilzeit
- Vitalwerte
- Englisch
- Patientenbehandlung
- Weiterbildungsprogramme
Sponsor-dedicated Project Manager Study Start up (m/w/d)
Fortrea —München
- Vollzeit
- Teamleitung
- Organisationstalent
- Kommunikationsfähigkeit
- Weiterbildungsprogramme
- Flexible Arbeitszeiten
Medizinische/-r Studienassistent/-in, Wecare (m/w/d)
Barmherzige Brüder —München
- Online-Bewerbung
- Krankenhaus
- Patientenbehandlung
- Recruiting
- Weiterbildungsprogramme
Study Nurse (m/w/d) zur Leitung der Studienambulanz
Universitätsklinikum Würzburg —Würzburg
- Vollzeit
- Blutentnahme
- Englisch
- Patientenbehandlung
- Weiterbildungsprogramme
- Flexible Arbeitszeiten
7 Tage
Study Nurse (m/w/d) / Studienkoordinator:in | 24 Std./Woche | Kempten
IQVIA —Kempten (Allgäu)
- Teilzeit
- Microsoft Word
- Forschungserfahrung
- Dateneingabe
6 Tage
Qualifizierung zur Studienassistenz
Universitätsklinikum Regensburg - Anstalt des öffentlichen Rechts —Regensburg
- Teilzeit
Direkt bewerben
7 Tage
Studienassistenz (m/w/d) in der Klinik für Gynäkologie und Geburtshilfe
Klinikum Bayreuth GmbH —Bayreuth
- 41.637,86 € – 50.451,67 € pro Jahr
- Teilzeit
- Krankenhaus
- Englisch
- Patientenbehandlung
Study Nurse (m/w/d)
Universitätsklinikum Würzburg —Würzburg
- Teilzeit
- Blutentnahme
- Englisch
- Patientenbehandlung
- Weiterbildungsprogramme
- Flexible Arbeitszeiten
7 Tage
Nurse
Job Trust —München
- 31.000 € – 42.000 € pro Jahr
13 Tage
Study Nurse (m/w/d)
BG Klinikum Murnau gGmbH —Murnau am Staffelsee
- Teilzeit
- Krankenhaus
- Weiterbildungsprogramme
- Empfehlungsprogramm
Study Nurse (m/w/d)
Klinikum Garmisch-Partenkirchen GmbH —Garmisch-Partenkirchen
- Teilzeit
- Englisch
- PC-Kenntnisse
- Weiterbildungsprogramme
Direkt bewerben
Gesundheits- und Krankenpfleger / Study Nurse (m/w/d) in Vollzeit
Nuvisan GmbH —Neu-Ulm
- Teilzeit
- Microsoft Word
- Blutentnahme
- Patientenbehandlung
Apprenticeship in Nursing
Haus der Pflege – KITZINGERLAND GmbH —Kitzingen
- 450 € pro Monat
- Teilzeit
- Nursing
MFA (m/w/d) - Interdisziplinäre Tumorambulanz (ITA)
TUM Klinikum Rechts der Isar —München
- Teilzeit
- Blutentnahme
- Patientenbehandlung
- Recruiting
12 Tage

Ich möchte aktuelle Job-E-Mails für Stellen als study nurse in bayern erhalten

Wenn Sie sich bei Ihrem Konto anmelden, stimmen Sie den Nutzungsbedingungen, den Richtlinien zur Verwendung von Cookies sowie der Datenschutzerklärung von SimplyHired zu.

Weitere Job-Standorte erkunden

study nurse jobs near bayern

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

study nurse Jobs in bayern

Ich möchte aktuelle Job-E-Mails für Stellen als study nurse in bayern 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.