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The Lead Clinical Data Manager coordinates data management activities for clinical trials, serving as the primary point of contact for internal teams, sponsors, and vendors. They are responsible for overseeing data review, ensuring audit-ready documentation, and managing project timelines and budgets.
The Lead Clinical Data Manager (LDM) is responsible for the coordination and delivery of Data Management contracted services on assigned projects. This includes meeting internal and external sponsor requirements according to time, quality, scope, and budget parameters. The LDM is the primary point of contact for Data Management on a project, for internal project team members, sponsors, and external data vendors. The LDM presents project-related training and may provide technical guidance and direction to team members. After initial training and onboarding period, this role is expected to work independently and proficiently, taking ownership of their assigned projects.
Essential Duties & Responsibilities
Serves as the primary Data Management interface for internal project team members, sponsor representatives, third party CROs and external data vendors
Ensures the timely initiation, conduct and completion of Data Management activities on clinical trials
Leads a sub-team of Data Management staff members assigned to a project
Tracks Data Management timelines for assigned projects and ensures that all applicable Data Management team members are aware and on target for deliverables
Authors the Data Management Plan (DMP), outlining all data management responsibilities
Develops and collaborates with the Database Builder to develop CRF specifications from the study protocol
Oversees UAT of clinical data systems (EDC, eCOA, IWRS) to be implemented on a project
Conducts and tracks internal DM team project-specific training throughout the course of the project, as needed
Attends and presents at project meetings as required
Oversees the completion of a comprehensive data review of clinical data
Ensures medical coding and/or Serious Adverse Event Reconciliation is performed in a timely manner
Assists with protocol deviation review and collaborates with project team on identified issues
Perform clinical data archiving duties as assigned
Ensures DM documentation is audit-ready and filed appropriately at all times
Coordinates all activities in preparation for database lock
Produces status or progress reports, listings, and other output as required during the course of the project
Monitors budget and scope of work for contracted DM services throughout the duration of the project, identifying out of scope or budget activities and collaborating with the project manager when out of scope documentation and costs are needed
Perform other duties as assigned by management
Qualifications
Bachelor’s degree in a related field of study or equivalent combination of education and work experience
Minimum 2 years experience in a lead role in Data Management preferred
CRO experience preferred
Working knowledge of data management process from study start-up through database lock
Understands how to prioritize deliverables and proactively address challenges with meeting deadlines
Basic knowledge of ICH/GCP standards, 21 CFR Part 11
Basic knowledge of GCDMP Guidelines
Proficiency in Microsoft Word, Excel, PowerPoint, Outlook, Teams and Zoom
Effective verbal and writing skills; English + local language, if relevant
Meticulous attention to detail
Time management and the ability to prioritize
EDC experience
Ability to travel <10%
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