Sr. Clinical Data Coordinator Job Duties : Support laboratory data management procedures including authoring and reviewing data transfer plans, overseeing data transfers, processing and storage of data. Use templates and standard guidelines to initiate documents but exercises critical thinking and discretion to tailor documents to study needs.
Support data cleaning activities for lab data reconciliation. Research and resolve discrepancies of moderate complexity.
Assist lead Biomarker Data Specialists to create detailed specifications for tabular and unstructured data by working with various stakeholders to ensure appropriate metadata variables and fit-for-purpose data structure meet end user needs.
With guidance, assist in managing multiple project streams by coordinating with internal and external stakeholders concerning timelines and deliverables. Internal stakeholders may include Clinical Pharmacologists, Biomarker & Bioinformatics scientists, Clinical Specimen Coordinators, Clinical Project Managers and others. External stakeholders may include vendor representatives such as Project Managers, Data Analysts and others.
Advise and coordinate with clinical project managers, scientists, external vendor contacts, programmers, analysts and other stakeholders regarding timelines and deliverables
Work with internal and external stakeholders to coordinate specimen testing in accordance with study plans and timelines.
Maintain an integrated tracking and inventory log of all specimens collected during a clinical trial, interpret data and share metrics with stakeholders.
Conduct data cleaning activities for vendor data reconciliation with minimal guidance. Exercise discretion and seek guidance as needed to choose efficient and effective issues resolution paths.
With some oversight, create detailed specifications for tabular and unstructured data by working with various stakeholders to ensure appropriate metadata variables and fit-for-purpose data structure that meet end user needs.
Run SAS programs, review SAS logs, and generate output.
Utilize problem-solving skills when working with vendors and collaborators to drive projects forward, seeking guidance when needed.
Draft, revise, and provide feedback on contracts and study documents to ensure alignment with stakeholders needs, internal processes and vendor capabilities.
Work with external labs and internal stakeholders to troubleshoot issues and implement process improvements of moderate scope.
Assist in maintenance of department tools, templates, and systems.
Sr. Clinical Data Coordinator • 95134 San Jose, CA, US
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