Minimum 3 years degree qualification.
- Promote and support the implementation of the Data Management
vision and strategy, including defining goals and objectives.
-Take full responsibility for all DM tasks, managing multiple trials.
-Provide leadership, management and coordination of data management operations and project deliverables (e.g. Review and provide input into Protocols, Operational Study Plan, Diaries and Questionnaires, Statistical Analysis Plan and Integrated Study Report, Data Management Plan, management of clinical trial data ,CRF design, CRF completion guidelines, database design, data entry, data cleaning, query management, documentation, serious adverse event and external data reconciliation, preparing validation plans and chairing validation meeting, review clinical data and clinical data processing, statistical activities and report and the clinical report)
-Ensuring productivity, efficiency and quality data management products in line with overall functional expectations that meet customer needs.
-Independently bring project solutions to the Data Management function.
-Assist with instruction, training and mentoring of Data Management
-Ensure resources are managed, including recruitment, training plans,
motivation and retention issues.
-Maintain high standard for the Data Management process including
Standard Operating Procedure responsibility.
-Research and propose initiatives for improving efficiency.
-Represent the Data Management function in International Clinical
teams and define project as well as trial level data.
-Track and report status and progress of Data Management for all trials and closely monitor timelines.
-Manage all projects in respect of: contracts, timelines, human resources, finances, etc.
-Be a backup for any one of the team.
-Main point of contact to the customer.
-Representing Company at various meetings and conferences.
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