Statistical Programmer (GCE) at IQVIA

Role overview:

• The Statistical Programmer is responsible for all statistical programming aspects for 1 or 2 studies with project-level activities. You will build and maintain effective working relationships with cross-functional teams, discuss deliverables, critical programming aspects and summarise activities as a member of the Clinical Trial Team.

Responsibilities & Requirements:

• Provide experienced technical expertise to develop process methodology for department to meet internal and external clients’ needs.
• Plan and coordinate the development of integrated programming solutions serving the full spectrum of statistical programming needs.
• Provide technical expertise and leadership to the department.
• Provide internal consulting services, including specifications and user needs analysis for complex project or client requirements.
• A crucial aspect is to maintain up-to-date advanced knowledge of programming software (e.g. SAS) as well as CDISC requirements (SDTM, ADaM, eCTD, Define.xml).
• Attend functional meetings and training.
• Minimum of 3 years of Statistical Programming experience within pharmaceutical or CRO environment.
• Strong ADaM and TFL experience required.
• Shadow lead for projects activities and collaborating with external clients.
• Excellent working knowledge of SAS and CDISC standards.
• Focus on communication, quality, timelines and highly technical.

Qualifications:

• BSc Degree in Life / Computer Science or Statistics
• Analytical and logical thinker with ideally a background working within clinical data programming.
• Strong communication skills, positive work aptitude and you must enjoy working with technology and data.
• Every employee has a personal development and career plan, and due to the growth of the company, the development potential is huge. We also offer an annual performance bonus, and a competitive benefits package.