Part of ETIC's, the first Belgian private network for health & safety at work, Vidyas offers training in the fields of well-being, prevention, and safety at work. Vidyas proposes also consultancy in prevention, safety and well-being at work.

BeCRO is a professional organization of Belgian Contract Research Organizations (CROs) which are supporting the pharmaceutical, biotechnology and medical devices industry in the clinical research and development of new products. The result of the combined industry efforts, including BeCRO members, is the availability of new treatments and therapies from which patients can benefit.

CONSULTYS is a global engineering and services consulting company exclusively dedicated to the biopharmaceutical industry. Since 2005 we handle major international biopharma’ technical projects. Our 520 consultants are currently working on innovative projects in engineering, production, quality (QA, QC, validation), R&D and regulatory affairs across Belgium, Switzerland, Canada and France. CONSULTYS is well-known for its values such as respect, transparency and performance. We truly believe in proximity management so that our consultants can develop technical competencies in a pleasant environment. Our wide range of biotech competences allows us to provide our expertise in all stages of biopharmaceutical industry lifecycle.

Keyrus Biopharma is an international full-service CRO with a reputation for transparency and integrity, highly focused on being able to deliver with excellence. Our ‘human’ approach to service provision is what differentiates us from our competitors. Combined with our high caliber staff, this approach has allowed us to become a key player in clinical research.Top talent, dedicated tools, integrated services and deep experience: our wide-ranging knowledge of clinical trials for pharmaceuticals, biotech, medical devices and vaccines … make us your perfect project partners!Targeting client requirements: whether external or in-sourced, for clinical or research applications … our services enhance your solution!

• Business development of Benelux, North of France: Insourcing, Outsourcing, Near-shoring intervention for Data Management including Safety, Biostatistics, Scientific Writing and Regulatory Affairs.• Follow-up of Existing accounts• Follow-up of insourced consultants at the client sites.

Consultant for GSK BiologicalsSenior Clinical Data Coordinator for Immunotherapeutic projects (mainly Oncology) and Prophylactics projects. Responsible for:• the quality and timings for clinical database• the coordination of Clinical Data Management activities• the communication between the actors (external/internal)• the development of CRF standards for Oncology projects

Responsible for a number of defined clinical applications (Oracle Clinical) and process developments (Data Standards). • Ensure that the Data Management systems/processes fulfill the role for which they have been designed/defined.• Maintain, develop and enhance in co-ordination with the end-users the clinical applications/processes• Coordinate the implementation, validation, training and maintenance of Oracle Clinical versions. • Support and facilitate development and upgrade of data standards (CRF, Database, Edit checks, CRF Guidelines)• Responsible of the Data Standards Steering Committee, planning meetings and taking and distributing minutes• Reviewing submitted data standards candidates, and ensuring that data standards governance and guidelines are being consistently applied.