Clinical Trial Assistant - CTQC (m|f|d)
Clinical Trial Assistant - CTQC (m|f|d)
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1 Vacancy
Job Description
As a Clinical Trial Assistant (CTA) in the Quality & Compliance (QC) area you play a key role in supporting the integrity and regulatory alignment of clinical trial documentation and processes. This role works closely with quality specialists to ensure that trials meet internal standards and external requirements.
- You update and maintain the trial documentation tools that track compliance ensuring they are accurate up to date and readily available to all stakeholders.
- You assist the CTQC Specialist in tracking and overseeing the completion of Corrective and Preventive Actions (CAPAs) across assigned studies.
- As a valuable member of the CTQC team you support in the preparation of and support during internal audits and regulatory inspections helping ensure smooth processes.
- Next to this you contribute to the maintenance of the Trial Master File (TMF) including document filing and organization and collaborate with CTQC TMF Specialists to uphold TMF quality standards.
- Also you actively participate in process improvement initiatives and support the revision and implementation of Standard Operating Procedures (SOPs) to enhance trial efficiency and compliance.
Qualifications :
- You hold a university degree in Life Sciences Natural Sciences or a related healthcare field and/or bring hands-on experience in clinical research ideally as a Clinical Trial Associate Clinical Research Associate or Clinical Study Coordinator within the pharmaceutical or biotech industry.
- Attention to detail comes naturally to you as well as being highly organized. You are used to prioritize multiple tasks to take initiative to work independently and to achieve project timelines.
- As a motivated and open-minded team player with well-developed interpersonal abilities you enjoy working in a dynamic environment. You are naturally communicative and have effective communication (verbal and written) and organization skills both in English. German is a plus.
- Your proficiency in MS Office and electronic clinical trial data management systems e.g. CTMS or eTMF is expected with an affinity for digital tools and dashboards.
- Finally you have a high attention to detail solution-oriented and proactive mindset.
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
Employment Type
Full-time
