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Associate Director, Clinical Database Programming

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15 MAY '23: For our client we are currently looking for an Associate Director, Clinical Database Programming. With a wealth of experience and expertise, this organisation plays a pivotal role in driving innovation within the healthcare industry. Dedicated to conducting high-quality clinical trials and providing comprehensive support services, this organisation focusses on guiding the innovative and starting biotech companies through the clinical phase of their drug development. Through their expertise and commitment they have been successful in advancing clinical trials that have the potential to transform patients’ lives.


Clinical Research

Clinical Research

Leuven - Belgium

40 uur per week

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Zo maak jij het verschil

You will be responsible for overseeing the development, maintenance, and compliance of database builds and Electronic Data Capture standards to support clinical studies. This includes tasks such as managing Edit Checks, CRF modules, and standard/custom reports. You will serve as a valuable resource for addressing database issues and providing problem-solving support related to clinical database technology, capabilities, and functionality. Identifying process deficiencies and proposing improvements to optimise clinical programming processes will be an important aspect. You will also contribute to the hiring, training, and evaluation of Clinical Database Programmers. Additionally, your involvement will extend to participating in the development of departmental SOPs and other relevant documents. Furthermore, it can be that you'll be invited to attend business development meetings.

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Wat jij mee brengt

As an Associate Director, Clinical Database Programming you have great attention to detail, and are able to work in a team environment with data-professionals. Moreover, you bring along:
  • Bachelor’s degree in computer science, mathematical science or related field;
  • 7+ years of experience in clinical database programming, preferably in a leadership role;
  • Extensive experience with the development, validation, execution, maintenance, documentation, and archival of clinical data targeted for regulatory submission;
  • Experience with Medidata Rave.

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Jouw voordelen

Besides the opportunity to join a growing team and become an essential link, this company offers:
  • Competitive base salary;
  • 30-32 vacation/leave days;
  • Meal vouchers & Eco vouchers;
  • Healthcare and group insurance;
  • Flexible work-life balance.


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