Clinical Trial Assistant (m|f|d)
Clinical Trial Assistant (m|f|d)
Employer Active
Job Alert
You will be updated with latest job alerts via email
Share
Job Alert
You will be updated with latest job alerts via email
Not Disclosed
Salary Not Disclosed
1 Vacancy
Job Description
As a Clinical Trial Assistant you will be supporting the Clinical Trial Manager in all aspects that are required to keep the quality and timeliness of study data and communication on a high level:
- You support the 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.
- Next this you support the preparation and submission of study documents to IRB/IEC and regulatory authorities and assist in the collection or creation and maintenance of study startup documents such as training materials logs and informed consent.
- You coordinate the filing and reconciliation of Trial Master File documents.
- In addition you support the study team by proactively identifying resolving and/or escalating issues to assigned staff.
- You assist with the creation and distribution of study-level communication to stakeholders and participate in internal team meetings taking minutes and providing status updates.
Qualifications :
- You have already gained experience in clinical research as a clinical trial associate clinical research associate and/or clinical study coordinator in the pharmaceutical/biotech industry and/or you are a holder of an academic degree in life sciences natural sciences or healthcare.
- Attention to detail comes naturally to you as well as being highly organized. You are 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 and German.
- Ideally you have already experience with hematological and/or oncological clinical studies and you are interested in cellular therapies.
- Your proficiency in MS Office and electronic clinical trial data management systems e.g. CTMS or eTMF is expected. Experience in Veeva ETM and CTMS preferred.
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
