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Clinical Trial Pharmacist (h/f)

Réf 1288001

Actualisé le 07 octobre 2020 par SGS BELGIUM

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At SGS, you can choose. First of all, out of our various vacancies. However, SGS also gives you another choice. Do you choose to expand or to enrich? We are not only looking for colleagues who can go in to depths of their discipline. We are equally as much looking for colleagues who we call `connectors¿, people who can connect our diversity to our services. To each other. And this way, enrich our business.

SGS is the world¿s leading inspection, verification, testing and certification company. We¿re also the benchmark worldwide for quality and integrity. And that makes us very proud. This can only happen thanks to almost 100 000 colleagues worldwide, with more than 1650 employees in Belgium only. Our employees give 110% of themselves every day, divided over all expertises, branches and cultures. Our coworkers build their own way inside the company, the services and the expertise.

SGS Life Sciences carries out all type of services for pharmaceutical and biotechnology companies, from coordination and running of clinical trials with new molecules or techniques on human beings, to support and consultancy on post marketing registration activities. SGS Life Sciences has also expertise in the quality control of pharmaceuticals. For our Clinical Pharmacology Unit (CPU) in Antwerp, we are currently looking for a Clinical Trial Pharmacist


In this role, you are responsible for the handling of Investigational Medicinal Products in a Clinical Trial Environment. This means you: Will be the primary Pharmacy contact to clients and the clinical trial team; Are an expert for trial medication. On top of that, you provide the division with support on several domains, whilst performing IMP handling such as accountability, storage, dispensing, ¿;   Are the colleague that will set-up the pharmacy related documents and IMP labels in line with sponsor¿s and regulatory requirements; Act as the problem-solver, you will follow-up corrective action plans towards deviations; Make sure everything is compliant for the Pharmacy services (e.g. developing, implementing and evaluating processes and procedures to ensure overall success). But that¿s not the only thing on your list. Additionally, you can also take up the role of Qualified Person. As a qualified person you will be responsible for quality control, certification, inspections, trainings, ¿ You will lead the Quality control of IMP at CPU. You make sure procedures are set out and followed, you select subcontractors, make sure people get the right training for the job, ¿ You are in control of incoming IMP materials (specification, testings, approvals); You check and double check the batch releases: are they compliant with environmental specifications, storage conditions, reference samples, etc¿; You make sure import and release IMP from outside EU can be used in clinical trials (ensure EU GMP manufacturing, certification of authorization documents, control of manufacturer information, QC analysis, release of IMP, keeping reference/retention samples);   And last but not least, you make sure the storage and use of IMP in clinical trials is assured.
  • Etudes, recherche et développement / Recherche fondamentale et appliquée

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