Clinical Trial Assistant (m/f/d) at Miltenyi Biotec

Bergisch Gladbach, North Rhine-Westphalia, Germany -

Full Time

Start Date

Immediate

Expiry Date

17 Feb, 26

Salary

0.0

Posted On

19 Nov, 25

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Clinical Research, Cellular Therapies, Analytical Skills, Organization, Flexibility, Prioritization, Initiative, Independence, Teamwork, Interpersonal Skills, English Communication, Microsoft Office

Industry

Biotechnology Research

Description

Company Description Miltenyi Biomedicine is a biopharmaceutical company committed to advancing personalized cell and gene therapies. We are pioneering groundbreaking therapies for serious life-threatening diseases, and reshaping their accessibility for clinical professionals and patients worldwide with the aim to improve and extend patients' lives. We are currently focusing on difficult-to-treat hematological cancers using CAR-T and other technologies, while also exploring treatments for other diseases. Our lead candidate, a tandem CAR T-cell product, is currently undergoing pivotal clinical trials on a global scale. Join our highly professional team in bringing new medicines to market and ensuring the safety of our pharmacological developments at all stages. Job Description Your role You are working in the department Clinical Development EU which is globally performing First-In-Man and Phase I-II Proof-of-Concept cell therapy clinical trials for our new assets. You support your team in all aspects that are required to keep the quality and timeliness of study data and communication on a high level. You assist with the preparation and distribution of study-level communication to stakeholders. You support distribution and tracking of critical clinical documents and information, e.g. essential documents, study supplies, budgets, manuals, other site and subject related information and investigational product releases in collaboration with the study team. You support the preparation and coordination of study related documents. You support the study team by proactively identifying, resolving, and/or escalating issues to assigned staff. You participate in internal team meetings, recording inputs and decisions (e.g. meeting minutes, etc.) and providing status updates. Qualifications Your profile You hold an academic degree (Master) in life or natural sciences/healthcare and you are interested clinical research and in cellular therapies. Your quick analytical skills are enabling you see the essence without getting lost in details and to make complex things simple. You are highly organized, flexible and you know how to prioritize multiple tasks on a regular base. You love to take initiative and to work independently in order to achieve project timelines proactively. Your motivation and engagement, your open-minded team play and well-developed interpersonal abilities are helping you to work in a dynamic environment. You are fluent in English communication (both in verbal and written) with very good presenting skills. A sound knowledge of Microsoft Office is a must have. Additional Information What we offer Working with free and self-determined time management, also mobile working An intercultural environment characterized by diversity and flat hierarchies Freedom to contribute creatively and play an active role in shaping the company Individual further training in our Miltenyi University as the core of the Miltenyi DNA 30 days of vacation, discounted ticket to Germany, (e)-bike leasing, capital-forming benefits, company pension plan, disability insurance, canteen, and much more. Diversity is the bedrock of our creativity Our mission: To innovate treatments and technologies and tackle the world’s most serious health challenges. And that’s why we connect the dots –across various disciplines, linking different perspectives, skills, and abilities. You and your talent are welcome here in our inclusive and collaborative environment. So come as you are. Regardless of gender, sexual identity, age, ethnicity, religion or disability. Become part of our team and focus on pushing the borders of medicine. We look forward to your application If you want to work in an open, creative and supportive team, this is the place for you. We look forward to receiving your application along with your salary expectations and availability.

Responsibilities

You will support the Clinical Development EU department in managing clinical trials, ensuring quality and timeliness of study data. Your role includes assisting with communication, tracking clinical documents, and participating in team meetings.