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Clinical Trial Supply Manager
il y a 3 semaines
CLINICAL TRIAL SUPPLY MANAGER
- Biopharma- Ghent & remoteWHAT IS OFFERED
We offer strong compensation packages that reward your abilities, hard work and ingenuity in achieving success.
We reward you with competitive wages and offer a strong package with additional legal benefits such as meal vouchers, eco vouchers, high health insurance (DKV) and group insurance. Depending on your seniority, a car may be provided.
We provide personalised training to let you grow in the area of
- What you like to do
- What you are good at
- Where and how you want to have an impact
ABOUT THE COMPANY
We offer the opportunity to:
- Take a front seat in the development of therapeutic antibodies
- Join a work environment in a human-sized, dynamic and rapidly growing biotech company
- Contribute to the build out of a global manufacturing network for innovative pharmaceutical product
- A competitive salary package with extensive benefits
- A flexible work environment with the possibility to work hybrid
Our partner is looking for a clinical trial support manager to expand their clinical study team. In this role you will be responsible for:
- Representing product supply in the clinical study team
- Driving development of clinical trial supply strategies and demand aligned with clinical trial protocols
- Collaboration with stakeholders and execute detailed clinical trial supply project plans
- Collaboration with the clinical study team and the CMC team
- Compliance to GxP requirements, local regulations and internal standards
- Create study specific pharmacy manuals and guidelines
- Actively tracking drug inventory
- Visualisation of active drug consumption and projected forecast
- Planning and organisation of global product manufacturing activities
- Responsible for management of external clinical trial supply vendors and distributors
- Collecting, registering and archiving information and documents in accordance with GCP guidelines
- Monitor and strengthen the clinical trial budget
REQUIRED COMPETENCES & SKILLS
- Master’s degree in a scientific discipline or equivalent through education and experience
- Minimum 4 years’ experience in field of clinical trial, preferably in clinical trial supply
- Knowledge of GxP regulatory requirements
- Quality conscience attitude; can do mentality
- Project management skills, good organization and planning skills
- Strong communication skills and able to build relationship with business partners and to work effectively together with others
- Flexible attitude, capable of picking up the tasks that require attention
- Working knowledge with MS Office package
- Fluent in English - our working language
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