Clinical Data Manager, Sr

KEY TASKS & RESPONSIBILITIES • Primary representative for eClinical Solutions/Sponsor data management interaction, ensure eClinical Solutions data management process is followed and deliverables meet quality and timelines within approved Scope • Senior technical resource providing Data Management services for project requirements including Protocol Conversion, Database Build, CRF design, Data Entry, Data Verification, Data Review, Query Management, Vendor Reconciliation • Define specifications and collaborate with technical team on configuration of centralized data management platform, elluminate Data Central for data cleaning strategy and oversight activities • Perform Quality Control on deliverables developed by team members including study documents, program and report specifications, deliverables and elluminate Data Central and analytics modules • Function as senior DM consultant to sponsor providing guidance on data management best practices as applied to sponsor and protocol specific situation • Perform data trending review via reporting and elluminate analytics to identify risks and develop mitigation and data cleaning strategies • Monitor and interpret key performance indicators (KPIs), dashboards, and reports to provide actionable recommendations to client • Delegate and prioritize tasks, provide project oversight and guidance to study data management team mentoring junior level staff and peers on all associated tasks within a study helping to grow individual capabilities • Support business development by participating in proposal defenses • Maintain project documentation related to assigned tasks • Other duties as assigned CANDIDATE S PROFILE Education & Experience • 8-10 years of experience in Clinical Data Management • Bachelor s degree in health-related field or equivalent experience Professional Skills • Strong project management experience and project team leadership skills including work planning and work delegation • Strong consulting and client relationship management skills • Detail oriented, ability to multitask with strong prioritization, planning and organization skills • Excellent verbal and written communication skills • Excellent team player • Excellent knowledge of English Technical Skills • Proficiency in Microsoft Office Applications, specifically MS Project and MS Excel • Knowledge of ICH/GCP guidelines, 21 CFR Part 11 and clinical trial methodology • Proficient with EDC and Clinical Data Management Systems • Experience with data reporting tools such as Qlik, JReview, Spotfire • Experience with RBQM methodology preferred Skills: Spotfire, Qlik, EDC, Ms Office Applications, Clinical Data Management, data reporting, Ms Project Experience: 8.00-10.00 Years