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• Pharmaceutical
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2.Ensures consistency on the design of trials within a program/indication
3.Maintains standards within a program/indication
4.Identifies trends in the data and possible solutions for efficiencies
5.With support from Program Clinical Data Manager (PCDM) ensures study conventions, processes, knowledge sharing and best practice exist for all assigned trials
6.Skilled on a range of systems/tools in use by Novartis and by Contract Research Organi-zation (CRO) partners and how to work with each accordingly
7.Effectively refines requirements for data validation based on metrics generated and les-sons learned from cleaning activities
8.Responsible for ongoing review of data, database maintenance & creation / maintenance of study documentation
9.Ensures the review of listings for quality, content, format and output
10.Supports & assists junior staff for assigned trials (e.g. raising data issues for Data Review Team (DRT) attention)
11.Responsible for the final review of data and finalization of the study documentation
12.Responsible for the final review of listings for quality, content, format and output
13.Tracks and reports status and progress for assigned trials, indications or programs. Is proactive to ensure timely deliverables (incl. Snapshots and interim/final locks).
14.Ensures appropriate tracking systems are kept up to date
15.Ensures creation of study specific project plans
16.Prepares feedback information about sites query performance and data entry compliance
17.Plans appropriately to ensure adherence to timelines, including assignment of workloads and identifying resource and timeline issues within and across programs
18.Interacts at International Clinical Teams (ICTs) and Biometrics and Data Management (BDM) Project Teams
19.Ensures adherence to GCP, DM standards, SOPs/Working Practices (WPs) and process guidelines
20.Able to effectively represent DM in SOP reviews and updates
21.Participates in Health Authority Inspections and assists in responding to requests for information from Health Authorities on DM related topics.
22.Responsible for managing all study documents required during a Regulatory or internal audit
23.Acts as cross-functional subject matter expert and presents at or chairs forums in areas of expertise
24.Mentors and trains new colleagues and/or other team members as assigned
25.Provides ongoing training and development of direct reports (if applicable)
26.Provides effective input into DM initiatives and innovations for quality, efficiency and continuous improvement in scientific and operational excellence
27.Proposes solutions to address resource and timeline issues
28.Provides ongoing input on performance of team members to next level manager
Minimum requirements Responsible and accountable for managing all Data Management deliverables with respect to cost, quality and timelines for all assigned programs, indications or trials managed within Clinical Data Management. Ensure consistently high quality data available for analysis and reporting.:
clinical data managementdocumentationcrosopdata entrygcpdata validationbiometrics internalaudit documents
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