Senior Clinical Research Associate I

TN Germany; München; Hybrid; EUR 50.000 - 70.000; Vollzeit

Zusammenfassung

A leading clinical research organization is seeking a Senior Clinical Research Associate I to enhance patient care through clinical studies. This role involves monitoring tasks, managing site communications, and training junior staff, with opportunities for professional growth and a flexible work environment.

Leistungen

Competitive salary and benefits

Flexible work environment

Extensive onboarding and mentorship

Growth opportunities and professional development

Qualifikationen

• Independent on-site monitoring experience in Germany.
• Experience in monitoring Phase II and/or III AMG studies.
• Experience in Oncology, Hematology, Infectious, Rare, or Gastrointestinal Diseases is a plus.

Aufgaben

• Conduct and report onsite and remote monitoring visits.
• Perform CRF review, source document verification, and query resolution.
• Manage communication with study sites.

Kenntnisse

Planning

Multitasking

Teamwork

Effective communication

Problem-solving

Proficiency in German

Proficiency in English

MS Office

Ausbildung

Degree in Life Sciences or equivalent

Jobbeschreibung

Social network you want to login/join with:

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Client:

PSI CRO

Location:

Job Category:

Other

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EU work permit required:

Yes

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Job Reference:

bc172d68565f

Job Views:

1

Posted:

20.05.2025

Expiry Date:

04.07.2025

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Job Description:

As a Senior Clinical Research Associate I at PSI, you will be involved in improving patients' lives through monitoring tasks and working on clinical studies across various therapeutic areas, maintaining high industry standards.

Office-based in Munich/Planegg or Home-based in Germany

You will:

• Conduct and report onsite and remote monitoring visits.
• Perform CRF review, source document verification, and query resolution.
• Manage communication with study sites.
• Participate in site identification processes.
• Assist in training less experienced CRAs, depending on your expertise.

Qualifications:

• Degree in Life Sciences or equivalent education and experience.
• Independent on-site monitoring experience in Germany.
• Experience in monitoring Phase II and/or III AMG studies.
• Experience in Oncology, Hematology, Infectious, Rare, or Gastrointestinal Diseases is a plus.
• Proficiency in German, English, and MS Office.
• Strong planning, multitasking, and teamwork skills.
• Effective communication and problem-solving abilities.
• Willingness to travel and valid driver’s license.

Additional Information:

As a privately owned mid-size CRO, we focus on company culture and operational excellence, offering growth opportunities and professional development. We provide extensive onboarding and mentorship, competitive salary and benefits, and a flexible work environment.

If you're interested in joining PSI and contributing to impactful clinical research, please apply for this vacancy.