Senior Statistical Programmer at DICE CRO

08/07/21

Location

Het Hofveld 6F, GROOT-BIJGAARDEN, Belgium

Function type

Programmer

Vacancy

We aim to enhance access to medical treatment

by delivering excellence in the design and execution of clinical trials.

 

Are you …

...looking for an entrepreneurial fast-growing company specialised in supporting interventional clinical trials where taking ownership and collaboration are key values?

…passionate about statistical analysis and aspire to play a crucial role in bringing new medical treatments to market?

 

Then check out this great opportunity to join us as a

Statistical Programmer

 

Who are we

DICE is a clinical research organization (CRO), that carries out all biometrics aspects of clinical research for pharmaceutical and biotechnology companies, from data management to processing statistical analysis and clinical study report compilation. DICE provides (electronic) data capture, data management, statistics, PK analysis, central imaging reviews, medical monitoring and medical writing services. Check us out on: www.dice-cro.com.

 

What makes DICE unique

  • We offer an entrepreneurial environment where you get to partner with start-ups as well as well-established companies. You will be instrumental in their success to bring new medicines to market safeguarding the correct process both from an ethical as statistical point of view;

  • You will be working on a variety of projects and contribute to different aspects ranging from design to final delivery;

  • We are committed to your continuous learning and development;

  • Collaboration and team spirit define our culture and strong values like service, excellence, integrity and ownership – ensure we deliver superior results for our customers.

 

What will you be doing

As a Statistical Programmer, you will be in charge of the statistical analysis of clinical studies.

 

This involves:

  1. Creation of data transfer specifications as per a blinding plan

  2. Reading data from external sources in SAS

  3. Integrate and reconcile all eCRF and external data into a clinical database. 

  4. Converting databases into the standard clinical formats like CDISC-SDTM and CDISC-ADaM

  5. Program data lists to support data management activities: edit checks patients lists, clinical coding, lab conversion and patients profiles

  6. Program lists for data safety monitoring boards and other independent committees

  7. Writing programs for the efficacy and safety analysis of clinical trials, based on the statistical analysis plan

  8. Program lists for regulatory submissions, for example, BIMO lists

  9. Consolidating the output of the statistical analysis in tables, figures and listings (TFL)

  10. Creating macros to automate tasks across projects

 

You will be part of a multidisciplinary and international team consisting of experts in statistical analysis of clinical trials.

 

Ideal work experience and education

  • Graduate degree in informatics or a Master Degree in a numerate field like Mathematics, Physics, (Bio-/Commercial-) Engineer or similar through experience. A degree in statistics is considered a plus

  • Minimum of 3 years experience in clinical research

  • Previous experience with SAS or R programming

  • Knowledge of the following is considered a plus:

    • CDISC CDASH, SDTM and ADaM

    • Knowledge of ICH and other guidelines in clinical research

  • Excellent verbal and written communication skills in English and Dutch or French

  • Good IT literacy: working with MS Office, Adobe, … has no secrets for you

  • Knowledge of Github or similar tools

  • you have proven to be capable of analytical thinking, either through education or experience.

 

What makes you stand out

  • Integrity

  • Focus with an eye for detail

  • Achievement orientation and high energy

  • Entrepreneurial mindset with a customer obsession

  • Can do attitude and the flexibility to engage in a variety of tasks

  • Growth mindset to continuously learn and stay on top of latest developments

  • The ability to work autonomously, as well as collaboratively in a team, in an atmosphere where giving constructive feedback is a must

 

What we offer

  • A competitive package with extra-legal benefits (company car, mobile phone, meal vouchers, and insurances package)

  • A young and dynamic work environment

  • A strong commitment to your professional growth and continuous development

  • An easy to reach office & possibilities to work from home

 

Your success will be the result of your entrepreneurial drive, passion for delivering superior results and your desire to fulfil the commitments to clients and co-workers.

Take your career to the next level, and apply now

Check us out on: https://www.dice-cro.com/

Send your applications to: elke.willaert@dice-cro.com 

Job application