Overview
We are currently seeking a Clinical Trial Manager* (CTM) to strengthen our Clinical Operations department. You will work in Tübingen/ Munich/ home-based (Germany) in an interdisciplinary global environment with colleagues from Germany and Houston (TX). Your analytical reasoning and action-oriented style as well as your organization and communication skills will contribute to the team’s success.
Your mission
Your main responsibilities will include but are not limited to the following tasks:
- Conduct and oversight of GCP compliant planning, execution and related clinical monitoring activities in clinical trials
- Conduct and oversight of clinical trial site selection processes
- Review of monitoring visit reports
- Oversight and coordination of deviations from clinical trials
- Relationship management and communication with the clinical trial sites
- Collection of clinical trial site specific documents for IRB/ IEC submissions according to local requirements and oversight of such
- Training of clinical trial sites and associated collaboration partners
- Performance review and management of clinical trial sites
- Conduct Sponsor Oversight Visits
- Develop and maintain SOPs, guidance documents & training material covering monitoring aspects
Your profile
You hold a Bachelor’s degree preferably in life science or nursing, or equivalent. You bring at least 4 years of on-site monitoring experience in the pharmaceutical/ biotechnology industry (incl. all monitoring visit types), and a comprehensive knowledge of ICH-GCP, FDA and EMA guidelines and applicable local regulations. You have already gained significant insights into Lead-CRA and/ or clinical trial management activities. Knowledge of basic medical oncology terminology and cell therapy is an advantage. Your competence, experience and project team leading skills enable you to successfully contribute to the management of our clinical operations. You are a good team player and role model with very good negotiation and resolution skills. Travelling up to 50% is acceptable for you.
We expect a high degree of independent working, analytical reasoning and excellent communication skills in German and English. 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. Your motivation is driven by excellence, efficiency and joy at work. 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.
