CDISC Data Manager

Frederick, MD
Aug 17, 2017
Aug 18, 2017
Full Time

The EMMES Corporation, organized in 1977, is a privately owned Contract Research Organization (CRO). Emmes is dedicated to providing statistical and epidemiological expertise, computer systems development, data management, study monitoring, regulatory guidance, and overall operational support to clients engaged in clinical and biomedical research.

Emmes serves as the Statistical and Data Coordinating Center (SDCC) for Clinical Research in Infectious Diseases (CRID) for more than 100 protocols sponsored by the National Institute of Allergy and Infectious Diseases’ (NIAID) Division of Microbiology and Infectious Diseases (DMID). Under the CRID contract, Emmes provides statistical, data management, and operational support for studies evaluating the safety, immunogenicity, and efficacy of vaccines and therapeutics against infectious diseases. These studies address critical public health needs to respond to emerging and re-emerging infectious diseases and potential agents of bioterrorism.

The Emmes CRID project is seeking a Data Manager with expertise in CDISC Study Data Tabulation Model standards to conduct SDTM mapping, review, and verification of conformance with current CDISC guidelines.

Primary Responsibilities

    Review protocols for CDISC conformance Develop and review Case Report Forms and eCRFs with CDISC CDASH and SDTM conformant elements Utilize proprietary Emmes software and mapping tools to annotate eCRFs and create data elements for SDTM output Review and verify SDTM data elements, SDTM annotations, and SDTM datasets and their conformance with the SDTM Implementation Guide, project standards, and the study protocol Create and review submission ready SDTM datasets, define.xml, and supporting documentation, as appropriate Provide CDISC training and serve as a subject matter support to project staff Perform other data management duties, including development and implementation of data quality checks, issuing queries, generating and QCing data reports and deliverables to the sponsor, as required


    Bachelor’s degree or Master’s degree with 2 years related experience, and demonstrated working knowledge of scientific principles appropriate to the position Excellent oral and written communication skills Prior experience with CDISC SDTM standards and application of standards to clinical trial data Documented training in CDISC SDTM, strongly preferred Prior experience with SQL and other database programming is preferred Strong interpersonal skills and ability to work with staff at all levels with sensitivity and tact Demonstrated ability to foster concepts of teamwork, research integrity, ethical conduct, and personal responsibility Ability to self-direct and work independently and in a complex team environment Knowledge of clinical research including the critical elements for the development and execution of clinical trials or research studies Strong skills in prioritization, organization, problem solving, decision-making, time management, mentoring, and planning

Emmes has an outstanding benefits package including: generous tuition reimbursement, professional development and training programs.


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Emmes is proud to be an Equal Opportunity Employer. EOE/M/F/D/V

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