Associate Clinical Trial Manager (m|f|d)

As an Associate Clinical Trial Manager you will support the Clinical Trial Manager in ensuring the successful planning execution and oversight of clinical trials at the country level. Your contribution will be essential to maintaining high-quality standards and meeting project timelines. 

• Act as the primary point of contact for specific assigned clinical trial sites coordinating all activities from start-up to close-out including CRO oversight. 
• Support the development and implementation of operational plans site trainings and study materials to ensure protocol compliance and enrolment success. 
• Monitor study progress contribute to enrolment strategies and escalate issues or delays to the Clinical Trial Manager or Group Leader as needed. 
• Review and manage essential documents (e.g. protocols informed consent forms) support Trial Master File (TMF) maintenance and ensure GCP and SOP compliance. 
• Collaborate with cross-functional teams (e.g. regulatory affairs medical affairs quality assurance logistics manufacturing and many more) and contribute to process improvements including the creation and revision of SOPs and templates.

Qualifications :

• We are looking for a proactive and communicative team player with a strong interest in clinical research and operational excellence. You thrive in a dynamic environment and bring a structured solution-oriented mindset. 
• Academic background in life sciences natural sciences medicine or a related field and proven experience in clinical research or clinical trial coordination ideally with exposure to Medical Affairs Clinical Operations or related functions. 
• Strong organizational and communication skills with the ability to manage multiple priorities and collaborate across teams. 
• Fluent in English and German; every other European language like French Spanish etc is a plus. Confident in using MS Office and clinical trial systems (e.g. CTMS eTMF). 
• Willingness to travel and engage with clinical sites and stakeholders; previous experience in hemato-oncology or cell therapies is highly valued. 

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 worlds most serious health challenges. And thats 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.

Remote Work :

No

Employment Type :

Full-time