Senior Clinical Research Associate (CRA)*

Immatics Inc; München; Hybrid; EUR 65.000 - 90.000; Vollzeit

Benefits dieser Stelle

Job bike

Job ticket

Health Programs

Childcare benefits

Relocation allowance

Company summer and winter events

Zusammenfassung

Immatics is seeking a Senior Clinical Research Associate (CRA) for full-time work across Germany, including Munich, Tübingen or remote options. You will monitor clinical sites, ensure GCP compliance, and support TMF/eTMF processes within an interdisciplinary team.

You should have a life sciences degree and at least 2 years of on-site monitoring experience in pharma/biotech, with strong German and English skills (C1) and willingness to travel up to 50–75%.

Qualifikationen

• Bachelor’s degree in life sciences, nursing or a comparable field and 2+ years of on-site monitoring experience in pharma/biotech.
• Deep knowledge of ICH-GCP, applicable regulations, and trial systems (eTMF, CTMS, EDC, IRT).
• Basic knowledge of oncology terminology and science; strong attention to detail and time management.
• Excellent presentation and communication skills in German and English (C1). Travel up to 50–75% expected.

Aufgaben

• Ensure clinical trial site management and monitoring in line with GCP, regulations, and SOPs.
• Execute monitoring activities: qualification, initiation, routine monitoring, and close-out visits.
• Maintain Investigator Site Files and Trial Master Files.
• Prepare timely visit reports and review trial progress; address issues.
• Coordinate with trial supplies, stakeholders and vendors.
• Participate in trial team, department and company meetings.
• Contribute to trial documents and improve Clinical Operations processes.

Kenntnisse

On-site monitoring

ICH-GCP knowledge

eTMF

CTMS

EDC

IRT

German language

English language

Travel willingness

Ausbildung

Bachelor's degree in life sciences or related field

Tools

eTMF

CTMS

EDC

IRT

Jobbeschreibung

OVERVIEW

We are currently seeking a full-time (40 hrs.) Senior Clinical Research Associate (CRA)* to strengthen our Clinical Operations department. You will work in Tübingen, Munich or remote within Germany in an interdisciplinary environment with colleagues from Germany and the US and will contribute to our mission of delivering novel PRAME immunotherapies to patients with cancer.

YOUR MISSION

The primary responsibility of this position is to ensure clinical trial site management and monitoring activities in compliance with GCP guidelines, applicable regulations, and SOPs, including: Execution of clinical monitoring activities, including qualification, initiation, routine monitoring, and close-out visits Maintenance of Investigator Site Files and Trial Master Files Implementation of site management activities in line with trial-specific functional plans Preparation of accurate and timely visit reports Review of trial progress (e.g., patient recruitment, data capture, issue resolution, etc.) and initiation of appropriate actions Primary contact for clinical trial supplies and other stakeholders or vendors Participation in clinical trial team, department and company meetings Contribution to the development of trial specific documents Contribution to the continuous improvement of Clinical Operations processes and procedures

YOUR PROFILE

You hold a Bachelor’s degree in life sciences, nursing or a comparable field and have 2+ years of experience in on-site monitoring (all visit types) within the pharmaceutical or biotechnology industry. In-depth knowledge of ICH-GCP, applicable regulations, and clinical trial systems (e.g., eTMF, CTMS, EDC, IRT) is required. Basic knowledge of oncology, including terminology and underlying science, is preferred. We expect a high level of attention to detail, strong time management skills, including independent prioritization, and a solution-oriented working style. You thrive in a dynamic, quality-driven environment and bring excellent presentation and communication skills in German and English (minimum C1 level). A positive attitude, strong team spirit, and willingness to travel up to 50-75% complete your profile.

WHY US?

We are the global leader in precision targeting of PRAME. Driven by our mission to make an impact on the lives of patients with cancer, we are a committed and inspired team and cherish the collegial, highly motivated, and family-friendly atmosphere within Immatics. Our culture allows for a high level of originality, independent thinking, and initiative. We believe in supporting our employees’ professional and social skills: We enable them to join conferences and trainings as well as to enjoy our Immatics benefits – e.g.,

• job bike


• job ticket


• Health Programs


• childcare benefits


• relocation allowance


• Company summer and winter events

Immatics N.V. and all Immatics subsidiaries are equal opportunity employers that evaluate qualified applicants without regard to race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity, or other characteristics protected by law.

ABOUT IMMATICS

Immatics is committed to making a meaningful impact on the lives of patients with cancer. We are the global leader in precision targeting of PRAME, a target expressed in more than 50 cancers. Our cutting-edge science and robust clinical pipeline form the broadest PRAME franchise with the most PRAME indications and modalities, spanning TCR T-cell therapies and TCR bispecifics. Immatics is committed to making a meaningful impact on the lives of patients with cancer. We are the global leader in precision targeting of PRAME, a target expressed in more than 50 cancers. Our cutting-edge science and robust clinical pipeline form the broadest PRAME franchise with the most PRAME indications and modalities, spanning TCR T-cell therapies and TCR bispecifics.