Senior Clinical Research Associate

We are currently seeking a full- or part-time (min. 30 hrs/ week), English and Dutch-speaking Senior Clinical Research Associate* to support our Clinical Operations team with monitoring visits in The Netherlands. This is a remote position based in Germany, with the role particularly well-suited to candidates located near the Dutch border. The role is offered through a fixed-term employment contract limited to two years.

You will work 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, national and local regulations or laws, and SOPs, including but not limited to:

• Performance of all aspects of clinical monitoring for clinical trials including site qualification visits, site initiation visits, routine monitoring visits and close-out visits at clinical trial sites

• Support in the maintenance of the Investigator Site Files and Trial Master Files

• Execution of all aspects of site management as outlined in the clinical trial-specific functional plans

• Preparation of accurate and timely trip visit reports

• Review of clinical trial progress, especially patient recruitment and clinical trial data capture, and initiation of appropriate actions to achieve objectives

• Primary contact responsibility for clinical trial supplies and other suppliers (vendors)

• Participation in regular clinical trial team meetings

• Proactive contribution to continuous improvement of Clinical Operations-specific processes, procedures, and templates

YOUR PROFILE

• You hold at least an apprenticeship or Bachelor's Degree (or equivalent), preferably in life sciences, nursing, or a related field, and bring 3+ years of on-site monitoring experience in the pharmaceutical or biotechnology industry, covering all types of monitoring visits.

• You have in-depth knowledge of ICH-GCP as well as applicable local regulations and laws.

• You bring proven experience in and a solid understanding of medical oncology.

• You demonstrate strong problem-solving skills, attention to detail, and the ability to work independently while effectively managing priorities.

• You show a collaborative mindset, openness to learning, and a proactive approach to contributing to innovation and continuous improvement.

• You possess advanced verbal and written communication skills in Dutch and English; German is a plus.

• You are proficient in Microsoft Office and clinical trial systems (i.e., eTMF, CTMS, EDC, IRT).

• You are willing to travel up to 75%.

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, Company summer and winter events.

NOTICE

*We value diversity and inclusion. 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.