Job Reference: BBBH23159
Job Duration: 12 Months
Start date: a.s.a.p
Description:
Required qualifications and experience:
-Life science degree in mathematics, statistics, informatics or related disciplines
-At least 3 years' experience in Pharmaceutical or Biotech industry within Clinical Research and / or Clinical Data Management with good level of functional expertise in Data Management
-Good knowledge of international clinical research regulations and requirements (e.g., International Conference on Harmonization
-Good Clinical Practice (ICH/GCP))
-Experience in clinical trial databases and applications, clinical data flow, data review, and (e)Case Report Form (CRF) design
-Ability to lead and coordinate the activity of DATA SCIENTIST(S) allocated to his/her study
-Goodorganizational and presentation skills
-Fluent in written and spoken English
Responsibilities and Tasks:
-Ensures that Data Management (Biometry) activities (related to assigned study) adhere to company standards, and applicable regulations
-Meet study timelines in terms of Data Management deliverables
-Ensure data handling consistency within allocated study(ies)
-Leads Data Management activities for assigned study
-Provide Data Management input to the development of the study protocol
-Coordinates the development of the (e)CRF in line with standards
-Writes all study Data Management documents covering specifications forexternal data transfer, data cleanings and review tools that will be further provided to DATA MANAGEMENT PROGRAMMER(S) for development for the allocated study(ies)
-Organizes, monitors and tracks the testing of data entry screens (eCRF layout), data cleaning / review tools, and their implementation in the production environment
-Organizes, monitors and tracks data cleaning, datareview, query management, and data-base lock; makes sure processes are driven in collaboration with key Clinical Development (CD) stakeholders
-Generates study metrics and status reports
-Represents Data Management at Clinical Trial Team (CTT) meetings-Manages and is accountable for Data Management activities in studies where Data Management is outsourced (insourcing/outsourcing partners' management)
-Prepares and archives Data Management study documentation
-Presents study related topics at CTT, Investigators and Monitors meetings
-Participates in development and review of policies, Standard Operating Procedures (SOPs), andassociated documents for Data Management
-Represents Data Management in cross functional working groups related to the system/ process
-Forecasts study team resource requirements
-Ensures Data Managers assigned to study have required training
-Ensures Study Data Tabulation Model (SDTM) deliverables (Including SDTM datasets, define.xml and annotated CRF) are created, validated and provided as per agreed timelines
-Performs and/or coordinates Quality Control (QC): Periodic operational checks to verifythat clinical data are handled according to protocol, applicable Quality System (QS) documents and GCP
-Work is expected to beperformed on the premises of
-Acts as DATA MANAGER for studies where no DM is assigned
Industry: Pharmaceuticals
Salary: €80 - €120 per hour
Salary Benefits:
Vacancy Type: Contract
Job Skills: data manager, data scientist, data management, basel, switzerland
Contact Name: Tim Barratt
Website: -
Direct Application URL: -