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Associate Clinical Data Manager
4 weeks ago
**Responsibilities**:
- Gather Study Set up requirements through discussion and communication with relevant stakeholders.
- Perform Database Set up and validation to ensure quality study design for data collection.
- Support validation of new Device integrations.
- Perform regular Data cleaning activities to ensure clean data with quality and timely deliverables to sponsor.
- Ensure that all the deliverables are of expected quality standards and meet customer expectations.
- Support Training of New joiners.
- Lead internal study meetings and internal/ sponsor audits and participate in Study Kick off meetings and other sponsor meetings.
- Tracks and manages the projects, oversee project progress, identify risks and take corrective action to rectify any errors as recommended by DTL.
- Manage the development and implementation of new technology / database revisions.
- Work closely with the programming team for process innovation and automation.
- Be compliant to trainings and eSOP reading.
- Provide review and expert opinion in developing, revising, and maintaining core operating procedures and working instructions.
- Communication with Line Manager, Leadership and other team members across functions should be collaborative.
**Skills and experience required**:
- Bachelor’s degree or educational equivalence in clinical, biological or mathematical sciences or related field OR a nursing qualification or equivalent combination of education, training and experience.
- Robust understanding of medical terminology and jargon required.
- At least 3 years of relevant experience in clinical data management.
- Strong EDC experience in clinical trials coupled with DM queries (familiarity with EDC platforms).
- SAS experience is not required, although good to have (database design).