Clinical Trial Supply Chain Manager
Posted 3 days ago by Park Street People
Negotiable
Undetermined
Undetermined
Uxbridge, England, United Kingdom
Summary: The Clinical Trial Supplies Manager will oversee clinical supply strategies for studies at a global pharmaceutical company in Uxbridge. This role involves managing timelines, liaising with vendors, and ensuring compliance with protocols and regulations. The position is initially for a 6-month contract and emphasizes innovation in pharmaceutical practices. Strong experience in clinical supply chains and drug development is essential.
Key Responsibilities:
- Manage clinical supply strategies within clinical studies whilst ensuring these delivered in a timely and cost-efficient 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
Key Skills:
- Strong knowledge of clinical supply chains and drug development processes (pharmaceutical industry experience is a pre-requisite need)
- Understanding of global regulatory requirements
- Previous experience in planning and managing clinical studies strategies
- Preferably, good knowledge of IVRS and CTMS systems
- Excellent communication and analytical skills
Salary (Rate): undetermined
City: Uxbridge
Country: United Kingdom
Working Arrangements: undetermined
IR35 Status: undetermined
Seniority Level: undetermined
Industry: Other
Our client, a global pharmaceutical company, is currently looking for a Clinical Trial Supplies Manager to join their team in Uxbridge on an initial 6-month contract. This is a great opportunity to work for a pharmaceutical company who have created a centre of excellence and constantly focus on driving innovation and using cutting edge techniques in their science.
Key Responsibilities
- Manage clinical supply strategies within clinical studies whilst ensuring these delivered in a timely and cost-efficient 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
- Strong knowledge of clinical supply chains and drug development processes (pharmaceutical industry experience is a pre-requisite need)
- Understanding of global regulatory requirements
- Previous experience in planning and managing clinical studies strategies
- Preferably, good knowledge of IVRS and CTMS systems
- Excellent communication and analytical skills
Park Street People Ltd is an Equal Opportunities Employer. We do not discriminate on the grounds of age, race, gender, disability, creed or sexual orientation and comply with all relevant UK legislation. We are acting as an Employment Business in relation to this role.