Senior Clinical Data Manager*
Here, you’ll achieve greatness.At BioNTech, you will be responsible for the quality of our clinical studies in the field of data management. Your duties in detail:
- Implementation and supervision of data management activities within assigned clinical trials
- Provision of adequate sponsor oversight to data management CRO’s or external data providers (e.g. for ePRO data, laboratory data)
- Monitoring and supervision of the set-up and maintenance of CDMS systems, eTools like EDC and filing and archiving of trial documentation
- Creation and execution of data quality checks
What you have to offer.
- Many years of professional experience in all relevant clinical data management activities in the pharmaceutical industry or CRO industry
- Experience in leading clinical data management activities on trial level and managing as well as supervising external CROs / vendors
- Routine in dealing with CDMS systems and eTools like EDC
- Sound knowledge of all relevant guidelines and aspects of clinical data management
Benefits for you.
Have we kindled your pioneering spirit?Then apply now for our location Mainz and simply send us your application documents using our online form.
If you have any further questions, Friederike Mangelsen will be happy to answer them on + 49 (0) 6131-9084-1291 (monday-friday, from 12 noon).
*BioNTech does not differentiate on the basis of gender, race, religion, color, origin, sexual orientation, disability, age and other protected status as required by applicable law. We are committed to creating a diverse environment and are proud to be an equal opportunity employer.
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