We are currently seeking a (Senior) Clinical Trial Associate* to strengthen our Clinical Operations department. You will work in an interdisciplinary environment with colleagues from Germany and Houston (TX, USA). Your analytical reasoning and action-oriented style as well as your organization and communication skills will contribute to the team’s success. The position can be located in Tübingen, Munich or remote (in Germany).

Your mission

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

Providing support for GCP compliant clinical trial planning, conducting and overseeing clinical trials
Keeping oversight, incl. but not limited to:
- tracking tools set-up and maintenance
- clinical trial documents preparation, review and/ or quality control
Providing support to the administration of clinical trials based on the oversight, incl. but not limited to:
- meeting organization
- preparation of meeting minutes
- coordination of review processes and signature retrieval
- preparation of the Investigator Site File template
- print/ arrange printing service
- collection of essential site documents and eTMF upload
Organizing investigator grant payments with global oversight of investigator grant payments
Supporting development and maintenance of SOPs, guidance documents & training material

Your profile

You hold a Bachelor´s or Master´s degree in a life science/ medical field or you have a comparable education. You already gained working experience in the clinical research area of a pharmaceutical/ biotech company. In addition, you have demonstrated skills in working with Microsoft Office and clinical trial systems (i.e., eTMF, CTMS). ICH-GCP knowledge is a plus.

We expect a high degree of independent working, analytical reasoning and very good communication skills in German and English (written and spoken). You embrace rapidly changing requirements with an open mind, think outside the box and show a high degree of flexibility in an environment which is marked by a constant striving for excellence. You approach tasks in a structured, reliable and foresighted manner, combined with an elevated level of individual responsibility, enthusiasm and strong social skills.

Why us?

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.

About Us

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.

This job is no longer accepting applications

See open jobs at immatics biotechnologies.See open jobs similar to "(Senior) Clinical Trial Associate*" b2venture.

See more open positions at immatics biotechnologies

Privacy policy Cookie policy