Vacancies

Spontaneous application

Medical Data Reviewer

The Medical Data Reviewer (MDR) is responsible for the review of patient data from study case report forms and to ensure completeness, consistency and robustness of the data towards its potential submission to regulatory authorities for the registration of the related vaccine.

Publication Manager

The Publication Manager is responsible for the delivery of peer-reviewed scientific publications for a project or project area (clinical, Epidemiology, Health Outcomes, etc.), in collaboration with a multi-disciplinary team of experts.

Real World Evidence Scientist

This posting relates to 3 positions:For Immuno RWE Contract Scientist : see RWE Scientist advert below, also open on Permanent role.For Neuro RWE Contract Scientist : see RWE Scientist advert below, temporary assignment only.For Early Immuno RWE Contract Scientist : see RWE Lead Scientist advert below, for temporary assignment only.

Clinical Biostatistician

Provision of a statistical service for the co-ordination & production of statistical outputs, development of analysis plans and reporting of results. As required, perform role of mentor on projects and act as Statistical Team Leader for single study projects.

Clinical Statistical Programmer

Co-ordination of the statistical programming for the review, reporting and transfer of clinical trial data.

Regulatory Affairs Consultant

To strengthen their team, Business & Decision Life Sciences is looking for RA experts to oversee the development, coordination, follow-up and strategic and operational management of regulatory activities associated with the development and life cycle of prophylactic or therapeutic drugs, at both national and international levels.

Quality Assurance Consultant

Business & Decision Life Sciences is regularly looking for Consultant with a Specialization in QA for his current projects with his various partner. 

Non-Clinical Statistician Consultant

Business & Decision is actively looking for (Bio)Statistician that will work on various topic either in our clinical biometrics team at Brussels or directly on customer's site in various project e.g préclinical, epidemological, industrial, QC analytical statistics

Clinical Lab Study Manager

Accountable for the delivery of one or more studies from protocol through to study report and archiving. These can be all types of study from First in Human to Phase IV