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Job summary
A pioneering biotech company is seeking a Senior Specialist in Clinical Supply Chain for its Oxford location. The role involves managing drug manufacturing, ensuring regulatory compliance, leading supply chain discussions, and developing clinical supply strategies. Candidates should have experience in pharmaceutical quality systems and project management, with a degree in a relevant scientific field preferred. The company values innovation and diversity, providing a collaborative environment.
Qualifications
- Experience in pharmaceutical quality systems, drug development, and clinical project management.
- Knowledge of IRT systems and industry standards like ICH GCP is desirable.
Responsibilities
- Manage drug manufacturing and ensure compliance with regulatory standards.
- Lead supply chain discussions and develop clinical supply strategies.
- Coordinate labelling, packaging, and distribution activities.
Skills
Education
Tools
Full details of the job.
Vacancy Name: Senior Specialist, Clinical Supply Chain
Vacancy No: VN672
Employment Type: Full Time
Location of role: Conshohocken, PA
Gaithersburg, MD
Oxford, UK
Department: Clinical Supply Chain
The Senior Specialist, Clinical Supply Chain will manage drug manufacturing and the clinical supply chain, ensuring seamless provision across the clinical portfolio. The role involves collaboration with internal teams to deliver clinical supplies compliant with regulatory standards and quality processes.
- Lead supply chain discussions and communicate effectively with stakeholders.
- Develop and implement clinical supply strategies for studies.
- Design labelling, packaging, and supply strategies to meet study and regulatory requirements while maximizing efficiency.
- Coordinate label text generation, translations, and approvals with CMC and Regulatory teams.
- Produce supply agreement documents detailing supply design and operations.
- Ensure supply strategies balance cost, risk, and effectiveness.
- Translate clinical protocols into demand forecasts and monitor budgets.
- Manage vendor relationships and oversee labelling, packaging, and distribution activities.
- Ensure regulatory compliance in documentation and procedures.
- Support system testing, troubleshooting, and inventory management.
- Provide training and guidance to team members and stakeholders.
Essential: Experience in pharmaceutical quality systems, drug development, and clinical study project management.
Desirable: Experience with IRT systems, managing CROs, oncology trials, GMP, and knowledge of industry standards like ICH GCP.
- Strong communication and presentation skills.
- Discretion, confidentiality, and high organizational skills.
- Autonomy, result-orientation, and effective time management.
- Team collaboration, flexibility, and technical proficiency.
Degree or higher in a relevant scientific field; Master's or PhD preferred. Proficiency in Microsoft Office and SharePoint.
Immunocore is a pioneering biotech company focused on developing T cell receptor-based therapies for oncology, infectious, and autoimmune diseases. We foster an inclusive environment committed to innovation and excellence, valuing diversity and integrity.
* The salary benchmark is based on the target salaries of market leaders in their relevant sectors. It is intended to serve as a guide to help Premium Members assess open positions and to help in salary negotiations. The salary benchmark is not provided directly by the company, which could be significantly higher or lower.