Senior SAS Programmer FSP, single sponsor-dedicated - home- or office-based, EMEA
Athens, Greece
πριν από 2 μέρες

As a Senior SAS Programmer in our sponsor-dedicated Flexible Solutions business unit, you are central to the successful delivery of complex clinical trials (phases I-III) for renowned, innovative and global top pharmaceutical companies.

Oftentimes you will have the opportunity to lead studies through various phases of the clinical development plan and support submissions, regulatory questions, publications as well as ad hoc and post hoc requests.

In this role, you will develop and validate SAS programs for data presentation, analyses, and provide programming support to your multidisciplinary global project team.

This position allows you to participate in the development of innovative new benchmark drugs for a wide variety of therapeutic areas such as oncology, cardiovascular, respiratory, neurological, diabetes, rare diseases, pain, immunology etc.

Your expertise and your work as a statistical programmer has a direct impact on improving the health and lives of thousands of patients around the globe every day.

Join us and see why more than 90% of the top 20 global pharmaceutical companies are repeat customers!

Your work location can be 100% home-based anywhere in EMEA or, if you prefer, in any of our numerous offices in the region.

What else can you expect from us?

Rewarding and meaningful work in an established, diverse, highly profitable and respected global company

Highly competitive compensation packages, including various local benefits such as pension contributions, complimentary health insurance plans, remote working allowances etc.

A genuine work life balance

Flexibility in working hours

A thorough onboarding with support from your personal mentor

A permanent employment contract with Labcorp Drug Development

Excellent training and career development opportunities, as well as support with advancing your individual education

Strong support from your Labcorp Line Manager and your team, as well as from more than 20,000 colleagues worldwide

Your responsibilities :

Review SAPs and TFL shells from a programming perspective

Advise on the development of complex TFL shells from a programming perspective

Develop and / or lead the development of complex specifications for SDTMs and ADaM datasets

Develop and maintain SAS programs to create SDTM and ADaM datasets and TFLs, and perform quality control of SDTM, ADaMs and TFLs

Produce / define XML / PDFs, Analysis Results Metadata (ARM), aCRFs and Reviewers Guides to support SDTMs and ADaMs

Respond to QA and client audits and support qualification audits

Identify and propose innovative ways to improve the efficiency, quality and productivity of clinical statistical programming at Labcorp

Maintain awareness of industry standards, global regulatory requirements, internal guidelines and Standard Operating Procedures (SOP’s)

Your profile :

Degree in a relevant field such as mathematics, life sciences, statistics, computer sciences, etc.

In lieu of the above : an equivalent completed vocational training and / or equivalent professional experience in statistical programming

Solid professional experience as a statistical programmer within a biotech, CRO or pharmaceutical company

Demonstrated knowledge of base SAS, SAS macros, SAS / STAT; demonstrated ability to debug SAS programs

Proven professional experience with SDTMs, ADaM datasets and TFLs

Strong organizational skills, an autonomous and collaborative work style, a curious mind and a keen attention to detail

Business fluency in English both verbal and written is a must


Labcorp is proud to be an Equal Opportunity Employer :

As an EOE / AA employer, the organization will not discriminate in its employment practices due to an applicant's race, age, color, religion, sex, national origin, sexual orientation, gender identity, disability or veteran status.

For more information about how we collect and store your personal data, please see our Privacy Statement.

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