Senior Manager, Investigational Medicinal Product (IMP) Management

Shionogi Europe; United Kingdom; On-site; GBP 70,000 - 90,000; Full time

Job summary

A global pharmaceutical leader in the United Kingdom is seeking a Senior Manager, IMP Management to lead the clinical supply chain for global trials. The successful candidate will manage projects ensuring compliant delivery of investigational medicines. Ideal candidates will have expertise in Interactive Response Technology (IRT) along with a strong understanding of GxPs. This role offers a chance to make a significant impact within a purpose-driven company focusing on patient-centric solutions. Apply now to be part of this mission.

Qualifications

• Experience managing clinical trial supplies in a global environment.
• In-depth expertise of GxPs (especially GMP & GCP).
• Excellent communication and problem-solving skills.

Responsibilities

• Lead the management of clinical supply chain projects.
• Utilise and manage Interactive Response Technology (IRT).
• Oversee label generation, packaging, and distribution.
• Collaborate with clinical, regulatory, and quality teams.
• Troubleshoot supply chain issues.
• Ensure compliance with GCP and GMP requirements.

Skills

Experience with IRT (such as RTSM)

Management of clinical trial supplies

Knowledge of GxPs

Analytical skills

Problem-solving skills

Fluency in English

Education

Bachelor’s degree in Life Sciences, Pharmacy, Chemistry, Engineering, or Health Science

Job 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.

Responsibilities

• 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 looking for 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.

Qualifications

• Experience with IRT (such as RTSM) or demonstrated technical proficiency in IRT is essential for success in this position.
• Proven experience in 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.