Beschreibung
Data Management Support - Clinical Data - Medical Devices
Our client is a leading manufacturer of medical devices.
For an initial 6 month contract they are seeking someone with strong data analysis experience to support and perform analysis of external studies using the internal tools, relating to multiple clinical studies (Virology - HIV, HBV, HCV, CMV and Blood Screening - MPX, HEV)
The successful candidate will have the following responsibilities:
- Provide technical inputs for data management plan (DMP) and creating data validation specification plan.
- Transferring raw data files into result data files using internal software (gCAT- growth Curve Analysis Tool).
- Developing JMP scripts application to statistically analyze data available from multiple clinical studies (Virology - HIV, HBV, HCV, CMV and Blood Screening - MPX, HEV).
- Developing and testing edit checks to ensure data consistency and resolving any discrepancy found.
- Ensuring secured data transfers of source data files from in-vitro diagnostics platform and tracking all data files received including other platforms.
- Entry of data in a validated clinical database and creating metric reports for the study teams.
- Ensuring appropriate archival of all Trials Master files in Electronic Documentation System.
Candidates should apply if they have the following experience:
- Data Analysis experience (ideally within the pharmaceutical/medical devices industry)
- Strong communication skills