Data Management
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Clinical Research Professional with 7+ years of experience, specializing in Clinical Data Management and clinical trials. Reliable, well-organized, resourceful, and diligent CDM leader offering acumen in Phase II and Phase III studies in different aspects of data management from study start up to database lock (DBL). Proficient in Electronic Data Capture (EDC) platforms such as Inform, Medidata RAVE, Veeva Vault.
Expertise in developing DMP, UAT testing, preparing CRF Completion Guidelines and Data Validation plan. Assisted in the random allocation of subjects to different study groups, ensuring the trial's scientific integrity via Interactive Voice Response Systems (IVRS) or Interactive Web Response Systems (IWRS). Liaise with the Principal Lead (PL), System Designers and other study stake holders involved in the project and communicate pre-construction information and health and safety needs of the Clinical study as it progressed.
Committed to applying in-depth knowledge to further innovate and advance clinical research methodologies.
