Responsible for independently leading data management study activities CRO oversight and driving deliverable timelines.
Strong knowledge of EDC builds utilizing RAVE.
Represents data management function on the Clinical Sub-team ensuring aligned expectations between the CRO and client for all data related deliverables especially in support of key decision points and regulatory submissions
Contributes influential leadership in collaboration with other client Stakeholders to ensure established milestones and deliverables are met with the highest degree of quality
Partners with appropriate stakeholders and CRO partners to mitigate and resolve risks.
Provides input to functional governance with client strategic suppliers.
Partners with appropriate stakeholders to resolves issues escalated from the vendor and/or cross-functional teams.
Participates in preparing function for submission readiness and may represent function in a formal inspection or audit.
Participates and represents function in formal inspections and audits as requested.
Ensure archival and inspection readiness of all Data Management Trial Master File (TMF) documents.
Ensures achievement of major data management and milestones in coordination with other functions the Therapeutic Area Units Clinical Operations Statistical Programming and Statistics.
Responsible for the planning and management of external Data Management budgets and timelines to ensure accuracy understand trends in variances and support continuous improvement in forecasting.
Acts as a process expert for operational and oversight models
Maintains SOPs process maps templates and timelines to support functions operational and oversight models.
May prepare metrics to support the functions KPIs.
Represents function in external professional initiatives and organizations such as SCDM CDISC DIA etc.
to identify industry best practice and increase the visibility of client.
Contributes to functional Continuous Improvement initiatives providing strategic direction and identifying key deliverables that meet timelines budget and are in alignment with company departmental or functional requirements.
Ensure compliance with own Learning Curricula corporate and/or GXP requirements.
Works cross-functionally to ensure the quality of the data in each database and on time delivery as well as quality of other data management deliverables.
Requirements:
Bachelors Degree in a science health related or information technology field required.
Minimum 6 years experience in Clinical Data Management with at least 2 as a Lead.
Strong knowledge of data management best practices & technologies as applied to clinical trials
Solid understanding of clinical trial documents (protocols statistical analysis plans CRFs study reports) and processes.
Strong knowledge of FDA and ICH regulations and industry standards applicable to data capture and data management process.
Strong knowledge of broad drug development process with expertise in the cross-functional interfaces with the data management function.
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