Immatics combines the discovery of true targets for cancer immunotherapies with the development of the right T cell receptors with the goal of enabling a robust and specific T cell response against these targets.
This deep know-how is the foundation for our pipeline of Adoptive Cell Therapies and TCR Bispecifics as well as our partnerships with global leaders in the pharmaceutical industry. We are committed to delivering the power of T cells and to unlocking new avenues for patients in their fight against cancer.

OVERVIEW

We are currently seeking a (Senior) Manager Clinical Sciences* to strengthen our Clinical Sciences department. You will work in Tübingen, Munich or remote (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.

This position is a fixed-term role of approximately 18-24 months as it covers a maternity leave.

YOUR MISSION

Your main responsibilities will include but are not limited to the following tasks:

• Acquire and utilize knowledge of clinical trial design to develop Clinical Trial Protocols and specific Trial Concept Sheets. Participate in discussions concerning scientific and procedural aspects of trial design.

• In collaboration with Medical Writing, Clinical Development, Clinical Operations, Clinical Data Management, Biostatisticians and other stakeholders prepare specific sections of Clinical Trial Protocols, Trial Manuals, Investigator Meeting Materials and other documents, as needed.

• Development of Patient Facing Material like Patient Information Sheets and Informed Consent Forms.

• Contribute to the design and development of Electronic Data Capture databases.

• Address Clinical Trial Protocol related questions from stakeholders and investigators with Medical Doctor supervision.

• Perform Patient Profile review with Medical Doctor supervision.

• Contribute to the design, preparation and/ or review of data listings, summary tables, Clinical Trial Reports, manuscripts, and scientific presentations or similar.

• Assist in the preparation and review of regulatory documents.

• Summarize and interpret scientific information available in published literature.

YOUR PROFILE

You hold a university degree in Biology, Clinical or Life Sciences, or a related field, and have gained at least 2 years of professional experience in the conduct of Clinical Trials within the healthcare or life sciences industry. Solid knowledge of GCP guidelines and a deep understanding of Clinical Development processes are essential. Experience with early-/ late-phase or pivotal oncological trials is required.

Your motivation stems from a strong interest in oncology clinical research and patient safety, with the ambition to make a meaningful difference for patients with cancer.

We are looking for a team player with excellent collaboration skills and the ability to inspire colleagues. Outstanding communication skills in English are required; German is an advantage. You approach changing requirements with openness and creativity, think outside the box, and demonstrate a high level of flexibility in an environment driven by a constant pursuit of excellence. A structured and reliable working style, combined with strong analytical thinking, completes 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.

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.