Clinical Database Programmer - SAS Programming

Worldwide Clinical Trials
Nottingham, GB
Closing date
24 Sep 2020

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Data Management / Statistics, Clinical Data Management
Full Time
Contract Type
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To co-ordinate and perform processes associated with the configuration, maintenance and validation of databases and database systems and associated applications.


Tasks may include but are not limited to:
  • To liaise with relevant staff to determine the allocation of tasks, to establish timelines, to report progress and any issues outstanding.
  • To review specifications for the set-up and modification of project specific data entry software (including edit check specifications).
  • Review validation plan for edit check and reconciliation check specifications.
  • Develop, test and run SAS programs for clinical data management. This includes programs for data validation and reconciliation checks, data listings and data transfers.
  • To configure database/eDC software (both internal and 3 rd party) for the use of DM, sponsor and sites
  • To perform testing of databases and related applications according to IT and Data Management departmental SOPs, both for initial set-up and maintenance.
  • To run database upload programs and to process any error reports.
  • To liaise with 3 rd party vendors to resolve issues, implement changes to software
  • To liaise with Sponsors or their designates on matters associated with the transfer of electronic data to or from the company, as defined by the Director, Data Management.
  • To support DM in the production and maintenance of system procedures and documentation
  • Assist with Quality Assurance and Audit requirements
  • Perform other duties as assigned. The duties and responsibilities listed above are representative of the nature and level of work assigned and are not necessarily all-inclusive.

  • Be able to demonstrate good written and verbal communication skills.
  • Be able to demonstrate a methodical and logical approach to problem solving and the ability to learn new tasks quickly.
  • Be able to work with close attention to detail
  • Be questioning about the validity of data being entered/extracted.
  • Be hardworking and efficient.
  • Possess good team working skills.
  • Key competencies in customer focus, delivering on commitments, building strong relationships, communicating and influencing, and embracing innovation and change.
  • The job holder must be computer literate and numerate with a willingness to adapt to various computer systems

  • Be educated to degree level
  • Have experience of Data Management Systems and Software
  • An understanding of CDISC SDTM standards
  • Experience of SAS programming language



Are You Seeking A Career With Purpose?

The time is right to join our growing team, consisting of 1,600 talented and dedicated employees from across the globe. We’re doing innovative and exceptional work each and every day. Our team is filled with purpose, as we support our sponsors in the discovery of cures and treatments for diseases affecting millions of people around the world.

If you’re looking to join an energetic and collaborative team that is valued and supported by company leadership, committed to operational excellence and open to creativity and innovation, Worldwide Clinical Trials could be the ideal place for you. We have exciting opportunities in clinical drug development, project management, corporate functions, sales, and more. Explore current openings and learn more about Worldwide’s culture below.

What We Believe

At Worldwide we operate under a shared mission, vision and set of cultural values. But these aren’t just words on a page. They are a daily inspiration and a shared commitment. Because we know that when we work towards a common goal and when we bring our best selves to the job every day we can climb mountains for our customers!

Contact Us
  • 2nd Floor
  • 172 Tottenham Court Road
  • W1T 7NS
  • GB
  • 0207 121 61 61
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