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
#J-18808-Ljbffr…