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Clinical/SAS Programmer (≥0.8 FTE/32 hours)

Are you an experienced Clinical/SAS programmer looking for a new opportunity? Clin-Q, a small and dynamic biostatistics and programming support company, is seeking an enthusiastic and motivated Programmer to join the team.

Clin-Q provides programming and statistical support for various pharmaceutical, biotechnical and medical device companies in EU, UK and USA. Clin-Q works in close collaboration with multidisciplinary clinical teams to provide the support needed.

As a Programmer at Clin-Q you interact directly with your colleagues, external consultants and clients, and you have an important role in creating programmed outputs. Due to the small size of Clin-Q, your role will be very diverse and requires a hands-on approach. At Clin-Q we all work closely together and support each other and our clients wherever we can, while at the same time we gain new learning experiences, improve collaborations and deliver impactful work.

Clin-Q embraces a healthy work/life balance and a flexible working time. We all work from home, and meet in person regularly. It is possible to work from the main office in Groningen, if that is preferred.

Job Overview

The Programmer supports the projects by miscellaneous tasks, including but not limited to: technical development, contribute to the creation of clinical documents, handle data transfers, CDISC/SDTM programming, CDISC/SDTM package creation, tables/listings/figures programming for inclusion in a Clinical Study Report, manuscript or regulatory submission packages. You are also able to coach other Clin-Q or external programmers with the project(s) and participate in writing/updating SOPs.

The Programmer is residing in the Netherlands or Belgium. The salary will depend on experience and location. Benefits include a pension plan, extra-statutory vacation days, vacation allowance, homework allowance, travel cost reimbursement and phone reimbursement.

Qualifications

– Residing in the Netherlands or Belgium;

– A BSc in a scientific or programming discipline (or comparable);

– At least 5 years demonstrated and relevant experience in SAS programming for clinical studies, with a preferred emphasis on programming for patient studies;

– Knowledge of R and/or Python is a plus;

– Relevant ICH-GCP and/or ISO training and knowledge of regulatory guidelines;

– Experience in CDISC/SDTM creation, or willing to learn;

– Experience in CDISC/ADaM creation is a plus;

– Able to support (Data Management) vendors in correct data delivery to Clin-Q;

– Experience in specific clinical areas (e.g. oncology, real world evidence, rare disease, medical device, pediatrics) is of interest;

– Able to work independently, and skills to provide active mentoring;

– Proficient communication and writing skills in English;

– Able to identify and develop new opportunities or technical improvements for Clin-Q;

Please do not send unsolicited services or offers.

Contact us to if you are interested in this position.