Description
We are looking for a
Clinical Data Manager (m/f)
Reference: -en
Start: asap
Duration: 24 MM
Place: in Baden-Württemberg
Branch: Pharmazeutische Industrie
Your tasks:
- Key liaison/data management lead to establish, align and confirm data management expectations for assigned trial(s)
- Responsible for CDM trial level oversight
- Build effective relationships with CROs/vendor partners
- Review protocols and identify requirements for proper data capture including electronic case report form design and processing of clinical data ensuring accuracy, consistency and completeness
- Oversee the design, creation and UAT plan and testing of clinical study databases along with development of edit check specifications and manual data listings as required
- Define or review creation and maintenance of all essential data management documentation
- Initiate and compile Trial Master File (TMF) relevant documentation containing the necessary CDM/Biostatistics & Data Sciences (BDS) documentation for a trial
Your qualifications
- Bachelor's degree or Master's degree (e.g. MBA, MSc) with major/focus in Life Sciences, Computer Science, Statistics or similar
- Experience clinical trial (data) management required
- Initial experience within the pharmaceutical industry, CROs or academic sites
- Technical expertise including industry data structure knowledge (e.g. CDASH/CDISC); EDC use and database specification experience
- Experience in using Statistical Analysis Software (SAS) programming
- Excellent in English
Skills:
- Clinical data manager