Curious? This would be your missions:
Under the supervision of the Responsible Pharmacist, you ensure the management of Investigational Products in line with Good Clinical and Distribution Practices :
- Assessment of the logistical and regulatory feasibility of the clinical study from a pharmaceutical point of view and participation in the implementation of studies in collaboration with the Sponsors;
- Participation in the proofreading of study documents related to pharmacy and provided by the Sponsor (pharmacy manual, dispensing protocol, clinical study protocol, ) before submission to the competent authorities;
- Participation in the initiation and monitoring visits organized by the Sponsor as a representative of the pharmacy department;
- Participation in the drafting or proofreading of documents related to the study according to the clinical protocol and the Pharmacy Manual (e.g.: medication preparation procedure, accountability logs, etc.);
- Organization of the dispensation of investigational products in collaboration with the Principal Investigator and the clinical team (project managers, study nurses, etc.);
- Ensure the good maintenance of the Pharmacy Binder documents and carry out regular data quality checks. Report deviations and ensure follow-up actions in collaboration with the quality department;
- Preparation of the investigational medicines / vaccines by strictly following the instructions described in the study documents;
- Ensure the proper management of equipment according to the procedures implemented at InoKura in collaboration with the quality department;
- Management of the daily stock and its Ensure the receipt and return of investigational Products.
Still interested? Let’s continue. The skills we are looking for in our new colleague:
- You hold a master degree in Pharmaceutical Sciences recognized in the European Union
- No experience is required but an interest in clinical research is essential
- You’re fluent in French and you have a good sense of verbal and written communication in English (minimum level B1, preferably B2)
- You have basic computer skills (word, outlook, excel,…).
- Hospital experience is a plus (ex: manipulations in a laminar flow hood)
- You are dynamic, proactive, motivated, autonomous, flexible.
- You are rigorous and organized
Do You project yourself easily? That’s our offer:
- A full-time or part time permanent contract based on hospital salary scale IFIC 17 with valuation of 7 euros of meal vouchers. 20 days off + 10 extra days.
- A daytime schedule from Monday to Friday between 8:30 a.m. and 17:00 p.m. with sometimes staggered hours in the morning (7:00 a.m. – 3:00 p.m.) + 20 days off + 10 extra days off.
Week-end hours are rare.
- A dynamic environment with renowned partners, at the forefront of pharmaceutical research
- Various missions in innovative therapeutic areas
- A human sized company (40 people) which allows you to develop your skills and initiatives
Contact :
Please send your CV and cover letter to rh@inokura.be