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Senior Manager, Investigational Medicinal Product (IMP) Management

Shionogi Europe

City Of London

On-site

GBP 70,000 - 90,000

Full time

30+ days ago

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Job summary

A global pharmaceutical leader is seeking a Senior Manager, IMP Management in London to oversee the clinical supply chain for global trials. This hands-on role requires expertise in Interactive Response Technology, extensive experience in the clinical trial supply chain, and a solid understanding of regulatory compliance. Join us in ensuring innovative treatments reach patients efficiently and compliantly.

Benefits

Dynamic and supportive environment
Opportunities for growth
Impact on public health

Qualifications

  • Experience with IRT (such as RTSM) is essential.
  • Proven experience in management of clinical trial supplies in a global environment.
  • In-depth expertise of GxPs, especially GMP & GCP.

Responsibilities

  • Lead the management of clinical supply chain projects from start to end.
  • Utilise and manage IRT to manage clinical supplies and participant enrolment.
  • Collaborate closely with clinical, regulatory, and quality teams.

Skills

Experience with IRT
Management of clinical trial supplies
Knowledge of GxPs
Analytical skills
Communication skills
Problem-solving skills
Fluency in English

Education

Bachelor's degree in Life Sciences or equivalent
Advanced degree desirable

Tools

Interactive Response Technology (IRT)
Job description

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Description

Shape the Future of Clinical Supply with Shionogi

At Shionogi, we are dedicated to protecting the health and well-being of people worldwide. As a global pharmaceutical leader, we are driven by science, innovation, and a deep sense of responsibility to public health. Join us in our mission to deliver life-changing treatments by ensuring the seamless management of clinical trial supplies across Europe and beyond.

Why Join Shionogi

Shionogi offers a collaborative, agile, and purpose-driven environment where your expertise can make a real impact. We value autonomy, adaptability, and operational excellence. This is a unique opportunity to contribute to a company expanding its footprint in Europe, with a strong focus on clinical development, supply chain innovation, and patient-centric solutions.

We are seeking a proactive and experienced Senior Manager, IMP Management to join our team in London. This role offers the chance to lead and shape the clinical supply chain for global clinical trials, ensuring that investigational medicines reach patients efficiently and compliantly.

About the Role

You will play a pivotal role in managing the clinical supply chain for global trials, ensuring timely and compliant delivery of investigational medicines. You will work closely with our colleagues in Japan, to lead and coordinate complex projects, collaborating with cross-functional teams.

As Senior Manager, IMP Management, you will:

  • Lead the management of assigned clinical supply chain projects, from protocol design through to study close-out.
  • Utilise and manage Interactive Response Technology (IRT) to manage clinical supplies and participant enrolment.
  • Oversee label generation, packaging, distribution (including CMOs), and IRT vendor management.
  • Collaborate closely with clinical, regulatory, and quality teams across Europe and globally.
  • Troubleshoot supply chain issues, including IRT and packaging logistics.
  • Ensure all clinical trial supply activities are completed in accordance with GCP and GMP requirements.
What Are We Looking For?

We are seeking a hands-on and strategic professional who can thrive in a fast-paced, global environment. The ideal candidate will combine technical expertise with strong problem-solving and communication skills.

  • Experience with IRT (such as RTSM) or demonstrated technical proficiency in IRT is essential for success in this position.
  • Proven experience of management of clinical trial supplies in a global environment, with knowledge of the full clinical trial supply chain.
  • In-depth expertise of GxPs (especially GMP & GCP) and regulatory compliance.
  • Excellent analytical, communication, and problem-solving skills.
  • Fluency in English, both written and spoken.
  • A Bachelor\'s degree (or equivalent) in Life Sciences, Pharmacy, Chemistry, Engineering, or other Health Science (Advanced degree desirable).
Join Us

Join Shionogi and be part of a team that is shaping the future of clinical development with purpose. We offer a dynamic and supportive environment, opportunities for growth, and the chance to make a lasting impact on public health. Apply now and help us ensure that innovative treatments reach the patients who need them most

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