Clinical Trial Coordinator

**Our mission**:
At Ethris, we are working at the forefront of medical innovation and technology. To us, this is a once-in-a-lifetime chance, working on rethinking human therapeutics. We strive towards developing the next generation of mRNA therapeutics and vaccines for respiratory diseases. We're a dedicated and skilled team of around 50 with different cultural backgrounds, all following the goal of revolutionizing medicine and bringing ground-breaking new therapies to patients worldwide in due time. With our truly innovative, self-developed and IP-protected suite of platforms for lipidoid nanoparticle delivery, mRNA design and optimization, mRNA manufacturing and drug product stabilization at room-temperature, we are uniquely positioned to achieve our ambitious goals.

**Our offer**
As a highly ambitious and thriving biotech company, we offer you an extremely interesting but also demanding job. You will have the opportunity to quickly expand your operational, strategic, and personal skills in a highly motivated team. An open communication culture and working atmosphere combined with a strong team spirit contribute to our success.

Join our team as **Clinical Trial Coordinator (M/F/x)**,** advance your career, and become part of an amazing journey to bring new and breakthrough genetic medicine to patients worldwide. You will play a key role in the operational execution of our clinical trials and will be part of **Clinical Operations.**

**Your tasks**:

- Assisting Clinical Operation functions with day-to-day logistics of assigned clinical trials, including project planning and status, coordination of meetings and internal & external communications
- Supporting trial team activities such as trial documentation management, milestone tracking and identification, resolution and escalation of issues
- Assisting with the operational feasibility of the protocols and assessment, selection and management of vendors; participating in strategies to ensure timely participant enrolment against the trial plan
- Assisting with the oversight of outsourced clinical trial activities and the development of trial related documents/plans and perform distribution/filing activities
- Assisting in the development of processes, document templates and procedures in order to ensure effective adherence to clinical trial regulations and guidelines

**Your profile**:

- 2+ years’ experience with clinical trials, either at site level or in the biotech/pharmaceutical industry or at a CRO
- Good communication skills and a good command of written and spoken English
- Knowledge of Good Clinical Practice, ICH guidelines
- A flexible, engaging, friendly and confident personality with a high level of initiative and ability to work independently
- Excellent interpersonal, written & verbal communication and organizational skills
- Detail oriented and achievement driven
- Aspirations for further development within the industry

**About us**:
Ethris is located in Munich, a very beautiful, exciting and safe city in southern Germany that offers a particularly high quality of life. The Munich region is considered one of the leading biotech hubs in Europe. Ethris truly benefits from the strong scientific cluster-knowledge in the region, driven by intense scientific exchange and collaboration with Munich’s renowned academic institutions, such as Ludwig Maximilian University, Technical University, Max Planck Institutes of Biochemistry and Neurobiology, and the Helmholtz-Center - as well as with other life science companies.