Keyrus Life Science is looking for a Clinical Trial Assistant to join our client's teams based in Liége on a hybrid model of 3 days on site and 2 days homeworking.

Your main missions are as follows:

• Preparation of investigator binders
• Ordering, shipping, stock management of the material under study
• Monitoring of sample transport
• Monitoring of administrative documents 
• Participation in updating study documents
• Maintaining the classification of documents relating to clinical trials
• Ensure the classification and archiving of paper and electronic study documents at TMF (Trial Master File) level, according to current procedures
• Participate in budget monitoring (invoices, contracts, insurance, etc.) for clinical trials
• Ensure at the end of the study the reconciliation of documents for closing and archiving

Education/Experience:

• Bachelor’s degree or equivalent and minimum 2 years of experience in industry (including pharma experience).
• Experience with clinical trials (phases 1 to 4).
• Proficient in MS Office (Excel), SAP is a plus.
• A scientific background is a plus.

Soft skills:

• Good organization skills.
• Stress resistant.
• Flexible, adaptive.
• Respect of deadlines and milestones.
• Good communication.
• Teamwork.
• Critical thinking.
• Proficiency in English (oral and written communication).

Area of Specialization:

• Good understanding of the clinical environment

Who we are

Keyrus Life Science is an international Consulting, Contract Research Organisation and Functional Services provider 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.

At Keyrus Life Science we’re proud of our commitment to delivering services of the highest quality, not only skilfully, efficiently and reliably, but also with sincerity and genuine care for our clients’ projects, priorities and reputation. Thus we maintain and advance our vision and our standards, all the while ensuring that we serve your interests better.

From early- to late-stage drug development, our range of services includes: Project Management, Clinical Operations, Pharmacovigilance, Quality Assurance (GxP), Regulatory Affairs Strategy & Support, Data Management, Medical Review & Coding, Biostatistics, Medical Writing & Medical Information, Real World evidence services.  

Keyrus Life Science is an inclusive employer that pays attention to applications from people with disabilities, to the career advancement of both men and women, and to the well-being of our LGBT+ employees.