Clinical Trials Supply Chain Specialist - Uxbridge, United Kingdom - Park Street People
Description
Our client, a global pharmaceutical company, is currently looking for a Clinical Trials Supply Chain Specialist to join their team in Uxbridge on a full time, 12-month temporary basis (35 hours per week).
You will be responsible for managing the supplies for the clinical trials and/or drug development whilst ensuring that this is done in a cost-effective and timely manner.
Key Responsibilities
- Manage clinical supply strategies within clinical studies whilst ensuring these delivered in a timely and costefficient manner
- Create clinical development timelines and proactively identify strategies and solutions for any issues that may arise
- Support the creation of medical protocols drafts and in the developing of package and label outlines
- Act as the clinical supplies point of contact and liaise with external vendors and services
- Ensure all products meet protocols and regulatory requirements
Requirements:
- Previous experience in a clinical development role within a pharmaceutical setting
- Strong knowledge of clinical supply and drug development processes
- Understanding of global regulatory requirements
- Previous experience in planning and managing clinical studies strategies
- Preferably, good knowledge of IRT and CTMS systems
- Excellent communication and analytical skills
We do not discriminate on the grounds of age, race, gender, disability, creed or sexual orientation and comply with all relevant UK legislation.
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