Professional | Permanent | Full-/ Part-time | Hybrid
If you’re passionate about changing lives for the better, this is the opportunity you’ve been waiting for. In Research & Development, we’re continuously exploring innovative new treatment options to make a stronger, more positive impact on the lives of the patients we serve. You’ll work with talented colleagues in a state-of-the-art Research & Development environment, developing innovative medicines that change the life of patients for the better and help us make progress towards our vision of a world free of pain. Join us today, and discover the difference you can make.
What The Job Looks Like
Each day you'll enjoy a variety of challenges, such as:
Being responsible for vendor relationship management and identifying potential external CTS service providers (e.g. Contract Manufacturing Organizations, Depots, Couriers, IRT providers)
Being the central point of contact for all trial supplies related activities for all assigned trials/projects
Developing trial‑specific packaging concepts in alignment with relevant stakeholders to achieve packaging design which ensures proper handling by site staff/patients and fulfils any blinding requirements
Developing of trial‑specific supply strategy including depot involvement to ensure in‑time delivery of high quality clinical trial supplies
Coordinating and overseeing manufacturing tasks, e.g. planning, coordination of bulk manufacture, packaging and labelling, coordination of QP release, storage requirements
Overseeing outsourced tasks related to any aspect of clinical trial supplies management to ensure adequate performance, implementation of risk management and issues are identified/communicated and corrective actions implemented and documented appropriately.
Maintaining and delivering budget oversight and forecasts
What You'll Bring To The Table
Pharmacist degree or comparable scientific, technical, or medical qualification
10 years‑experience in Pharmaceutical Industry in field of Clinical Trial Supply Management, preferably CRO experience
Experience in budget forecast and budget tracking
Experienced in the conduct of clinical trials
Thorough understanding of applicable EU and US GMP regulations for IMP manufacturing
Thorough understanding of GDP requirements for setup of logistical part of supply chain and of GCP requirements in the conduct of Phase I – IV trials
Excellent analytical, organizational and communication skills
Service‑oriented mindset whilst enjoying working in interdisciplinary teams
In this pivotal role, you will lead all aspects of clinical trial supply as part of a highly collaborative, cross‑functional team, working closely with internal teams and external vendors. Join us on our exciting journey towards a World Free of Pain.
Rachel Bramley, the Hiring Manager
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