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SAS Data Programmer (Office-Based) - IQVIA Biotech (R1083134) in Morrisville, NC at IQVIA™

Date Posted: 6/12/2019

Job Snapshot

  • Employee Type:
    Full-Time
  • Date Posted:
    6/12/2019
  • Job ID:
    R1083134

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.

We are seeking candidates that can manage and support project programming activities and deliverables focusing on specifications and programs to generate site payment reports and support site payment team.
Perform additional tasks such as programming SAS edit checks, vendor data reconciliation, vendor DTA, EDC extracts, and medical coding as needed. Additional responsibilities include work planning, attendance of internal and Sponsor meetings if needed, filing project documentations to TMF.

BASIC FUNCTIONS:

Perform lead responsibilities on one or more projects.  Develop and validate programs to generate data cleaning reports and prepare data extracts. Provide programming support to project team members and others within Project Programming.

ESSENTIAL JOB FUNCTIONS, DUTIES AND RESPONSIBILITIES:

  • Perform as a SAS Data lead for projects
    • Draft, update and maintain the Master Plan for assigned project and review study plans for other departments.
    • Review and provide feedback on project timelines and ensure that project tasks are completed timely and with acceptable quality
    • Manage study sFTP site accounts
    • Assume responsibility for project budget and perform monthly time projections.
    • Attend internal team meetings and relevant client team meetings, as needed.
    • Review data transfer specifications and test transfers from external vendors as applicable for reconciliation purpose.
    • Review and provide/collect SAS feedback on eCRF development and data structure changes and evaluate the impact on programming activities
    • File documentation associated with client delivery on an ongoing basis and perform final archival activity at study close.
  • Manage and support project programming activities and deliverables
    • Develop specifications/test data and program custom data files, SDTM and data integration as requested by Sponsor; update blank CRFs with SDTM or other custom annotations, develop define.xml file for SDTM.
    • Set up default clinical data transfer and/or perform scheduled and ad-hoc data transfers
    • Define specifications/test data, program and generate reports to facilitate vendor and/or SAE reconciliation, medical coding, investigator payments, data review (e.g., SAS data checks and patient profiles) and other needs, as requested.
    • Define specifications and test plans for data imports.
    • Develop specifications and programs to integrate local lab normal ranges with data extract.
    • Set up project-specific J-Review system for InfoLink and/or InForm.
    • Support programming activities for medical coding group, including integration of coded terms with data extract files.
    • Develop QC test plans, perform independent unit testing, complete documentation for SAS code installs and utilize source code management software.
  • Project Programming departmental responsibilities
    • Assist with process improvement initiatives, as agreed to by management.
    • Perform other duties that may be requested by management as assigned.

KNOWLEDGE, SKILLS AND ABILITIES:

  • Understanding of GCP, ICH, and FDA guidelines and regulations applicable to conduct clinical research.
  • Knowledge of programming and validation methods, and software development life cycle.
  • Knowledge of relational database concepts, and SQL experience.
  • Experience with SAS Base, SAS Macro, and ODS as well as strong data step skills.
  • Ability to perform multiple tasks efficiently and accurately with minimal supervision while meeting deadlines.
  • Ability to work independently and part of the team.
  • Ability to learn new programming languages, technology, tools and processes.

CRITICAL JOB FUNCTIONS IN ACCORDANCE WITH ADA CRITERIA:

  • Very little physical effort required to perform normal job duties (unless otherwise indicated)

MINIIUM RECRUITMENT STANDARDS:

  • BS degree (or equivalent, based upon education and experience) in Computer Science, Mathematics, life/analytical sciences or related field, and 2 years of work experience in SAS programming, preferably in a clinical environment, or
  • Masters-level degree in Computer Science, Mathematics, life/analytical sciences or related field with a minimum of 1 year of work experience in SAS programming, preferably in a clinical environment.
  • Excellent communication, interpersonal, and organization skills, highly detail-oriented.

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: R1083134