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Clinical Data Analyst (Office-Based) - IQVIA Biotech (R1082661) in Morrisville, NC at IQVIA™

Date Posted: 6/6/2019

Job Snapshot

  • Employee Type:
    Full-Time
  • Date Posted:
    6/6/2019
  • Job ID:
    R1082661

Job Description

IQVIA™ is the leading human data science company focused on helping healthcare clients find unparalleled insights and better solutions for patients. Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness the power of healthcare data, domain expertise, transformative technology, and advanced analytics to drive healthcare forward.

BASIC FUNCTIONS:

Perform project-specific system setup and testing, data analytics, reporting and script development/execution in support of SAS programming and other project team efforts.

ESSENTIAL JOB FUNCTIONS, DUTIES AND RESPONSIBILITIES:

CDPS Development:

  • Gather sponsor requirements and develop or review clinical data file (CDF) specifications.
  • Write or review CDF test data specifications and coordinate the data entry effort.
  • Perform scheduled and ad-hoc data transfers.

Integration and reconciliation of data transfers:

  • Work with vendor to define specifications for transfer of data from vendor to IQVIA Biotech.
  • Define specifications for import of data to CDPS, and /or back-end integration with CDF< as applicable.
  • Coordinate with Data Manager to define appropriate reconciliation report specifications.
  • Coordinate with Biostatistics/SAS programming staff to define appropriate test case scenarios, and review to ensure the accurate programming of data integration and reconciliation reports.

Aggregate data checks and other data review activity:

  • Set up project-specific I-Review system, including standard and custom views.
  • Provide custom query results and reports to data reviewers.
  • For those studies where contracted, perform ongoing aggregate-level review of data, to identify trends and areas of concern for data quality.

Site Payment systems:

  • Write or coordinate development of test data specifications, and coordinate data entry effort.

Other reporting development:

  • Write or coordinate development of test data specifications, and coordinate data entry effort.
  • Develop and/or validate programs to generate reports.
  • Assist the Manager in developing scripts and tools to facilitate the processes and work flow for Clinical Reporting, and other departments within Data Operations.  Collect user requirements, develop scripts, unit test, develop user documentation, and implement generic scripts and tools.
  • Perform scheduled and ad-hoc SAS administrative tasks.
  • Perform other duties as assigned.

KNOWLEDGE, SKILLS AND ABILITIES:

  • Knowledge of programming and validation methods, and software development cycle
  • Knowledge and/or experience with relational databases, reporting, or data mining
  • Knowledge of SQL, knowledge or exposure to SAS/Base programming
  • Experience with MS Office tools such as MS Word, Excel, and Access
  • Knowledge of clinical research process and methodology
  • Understanding of current GCP, ICH, and FDA guidelines and regulations applicable to conduct of clinical research
  • Ability to plan long-range needs while assuming responsibility for daily details with a high degree of accuracy
  • Ability to work creatively and independently to carry out assignments of a complex nature
  • Ability to communicate and work effectively and cooperatively with other professional staff members
  • Excellent organizational and program documentation skills, highly detail-oriented
  • Ability to learn new programming languages, new technology, and new tools that will facilitate the clinical trial process

MINIMUM RECRUITMENT STANDARDS:

Degree requirements include one of the following:

  • High school diploma with a minimum of three years work experience in programming; or
  • Associate degree, with a minimum of one year work experience in programming; or
  • Bachelor’s degree in Computer Science, Mathematics or equivalent 

Join Us

Making a positive impact on human health takes insight, curiosity, and intellectual courage. It takes brave minds, pushing the boundaries to transform healthcare. Regardless of your role, you will have the opportunity to play an important part in helping our clients drive healthcare forward and ultimately improve outcomes for patients.

Forge a career with greater purpose, make an impact, and never stop learning.

IQVIA is an EEO Employer - Minorities/Females/Protected Veterans/Disabled

IQVIA, Inc. provides reasonable accommodations for applicants with disabilities.  Applicants who require reasonable accommodation to submit an application for employment or otherwise participate in the application process should contact IQVIA’s Talent Acquisition team at workday_recruiting@iqvia.com to arrange for such an accommodation.



Job ID: R1082661