Everest Clinical Research · 1 day ago
Principal Data Manager I
Bridgewater, NJ
Full-time
Remote
Senior Level, Lead/Staff
10+ years exp
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Responsibilities
Act as the primary contact person for communication and discussion of topics related to data management timelines and deliverables; requests for out-of-scope tasks; and first line contact for technical or procedural issues.
Perform hands-on data management tasks including, but not limited to, writing database design specifications, test plans for user acceptance testing (UAT), and data transfer specifications. When these tasks are assigned to Data Management support team members, the Principal Clinical Data Manager is responsible for review or to provide data management oversight and approvals for the task performed to ensure quality deliverable, including review of UAT plans to ensure accuracy and consistency among projects. Facilitate and participate in UAT, as necessary.
Review data, issue queries, and resolve queries from various data sources (e.g., medical coding, medical history, adverse events, procedures and medicinal products, and external data). Assist other Clinical Research Organizations, Sponsor, or Investigative Sites with resolving queries.
Perform third party non-Case Report Form data management activities.
Plan, manage, and perform data processing and data management activities for assigned projects to ensure tasks are performed in a timely manner and in compliance with trial Sponsors’ requirements.
Accurately and efficiently validate electronically captured data. Lead efforts in writing clear queries on missing data and data points failing pre-defined range checks and/or logical checks.
Validate and disseminate real-time study monitoring reports to Sponsor and internal team members.
Review database edit check specifications for assigned studies. Lead efforts in developing and maintaining standard database validation checks for common modules as well as for therapeutic/drug area specific modules.
Perform training on the electronic data capture (EDC) system, dataflow, and quality control (QC) processes to clinical trial personnel.
Participate in project kick off meetings, investigators meetings, and regular project management team meetings.
Perform study-level resource planning and management, including the review of team members’ timesheet reports.
Manage the process of database modifications (after go-live) due to protocol amendments or study needs.
Develop and maintain the Data Management Plan (DMP). Document deviations from the DMP.
Assist in development and implementation of clinical data standards, training standards, project management, and data management technologies.
Develop and maintain the Data Quality Review Plan (DQRP). Coordinate with programmers to complete the programming and validation of the listings and summary tables as specified in the DQRP.
Assist in the development of project bids, billing, tracking of out-of-scope tasks, and participate in bid defense meetings.
Perform project tracking and maintain project milestones and timelines. Report and resolve any issues with defined timelines and deliverables to the next line of management.
Promote effective project management practices. Review and assess timesheet summary reports for assigned projects.
Follow up on regulatory requirements, industry trends, benchmarks, and best working practices in data management by reading and participating in relevant training and/or association activities.
Participate in and contribute to CDM departmental improvement initiatives.
Define and monitor clinical trial data flow and QC processes in accordance with corporate Standard Operating Procedures, Good Working Practices, and departmental guidelines.
Provide training to study site and Sponsor personnel on data entry and review (electronic data capture studies), data flow, and QC processes.
Cooperate and assist the Quality Assurance (QA) department with QA audits on assigned databases.
Ensure project team maintains and prepares final archival of data management documentation relevant to the assigned clinical trials and assist the corporate archivist in assembling and archiving such documentation.
Qualification
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Required
M.Sc. or B.Sc. in a related field.
Ten (10) years of related experience.
Demonstrated an in-depth understanding of clinical trial data management concepts, processes and procedures, relevant issues related to or impacting clinical data management, as well as pharmaceutical clinical trial regulations, industry guidance, conventions and standards.
Demonstrated leadership ability to effectively manage clinical trial data management activities and integrate them with the entire clinical trial operation.
Must communicate effectively, orally and in writing, with personnel on all professional and administrative levels.
Excellent presentation skills and the ability to build relationships with both internal and external clients.
Demonstrated ability to effectively organize and integrate the activities of information processing.
Must be well organized, able to work independently, and manage multiple projects/tasks appropriately.
Demonstrated knowledge of Data Management processes and data flow with the skill to ensure quality delivery.
Company
Everest Clinical Research
Everest Clinical Research is a firm which conducts clinical research by contract for firms across the globe in fields
501-1,000 employees
H1B Sponsorship
Everest Clinical Research has a track record of offering H1B sponsorships. Please note that this does not
guarantee sponsorship for this specific role. Below presents additional info for your
reference. (Data Powered by US Department of Labor)
Distribution of Different Job Fields Receiving Sponsorship
Represents job field similar to this job
Trends of Total Sponsorships
2023 (4)
2022 (3)
2021 (1)
Funding
Current Stage
Late StageTotal Funding
$0.1MKey Investors
FedDev
2020-12-07Acquired· undefined
2019-08-18Grant· $0.1M
Recent News
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