BE - R and D - Trial Supply Manager - Normal
This vacancy has now expired. Please see similar roles below...
An internationally renowned pharmaceutical company is currently advertising a Trial Supply Manager to their office in Beerse. This top 10 pharma company works across multiple sectors, including medical devices, pharmaceutical research, and consumer health. The vacancy offers an exciting opportunity to work with a company with over 100,000 professionals around the globe.
Job Responsibilities:
- Responsible for the management of clinical supplies during the execution phase of clinical trials consistent with GMP guidelines.
- Adapt supply strategies in view of changes in trial execution and ensure a seamless transition from study design phase.
- Assess clinical study recruitment rates and ensure supply planning is adapted accordingly.
- Utilize business tools to manage inventories at depots and sites and ensure on-time delivery with minimal overage of clinical supplies.
- Conduct issue resolution activities for supply aspects of clinical studies (e.g., packaging, distribution).
- Establish and modify trial specific distribution agreements
- Member of appropriate GCDO clinical trial team.
- Develop strong internal collaboration with GCDO stakeholders to ensure customer satisfaction.
- Interface with GCDO stakeholders at both the Trial and Compound level
- Develop excellent working relationships with the other groups within Supply Management. Manage trial supply budget.
- With guidance, manages the activities required to meet First-Patient-In date of clinical trials. This includes initial demand forecasting, configuration of the distribution network, IVR / RTSM specifications, and developing supply strategies to meet clinical plans while optimizing drug overage. Updates therapeutic area representatives on relevant clinical supply chain topics.
- With guidance, responsible for managing all aspects of issue escalation and resolution at the study level.
- Responsible for making transparent any study risks via the cS&OP process.
- Responsible for developing scenario analysis to drive/support decision-making through the cS&OP process.
- Escalation point and interface with the management team via Executive cS&OP, with guidance from Team Lead Focus and scope
- Responsible for the management of all clinical supplies during trial execution within J&J Pharma R&D (large and small molecules and for all phases of clinical trials).
- General focus on large, complex studies.
- Act as role model within team for use of core processes and proper use of systems and tools
- Takes accountability for own performance and development seeking opportunities to broaden knowledge and subject matter expertise.
- Support business process improvement initiatives.
- Gathers diverse viewpoints and able to influence key stakeholders within the Clinical Supply Chain, and other key cross functional partners.
Skills and Requirements:
- A minimum of a bachelor's degree is required.
- A minimum of four + (4+) years of relevant professional experience is required, preferably in a clinical supply related role.
- General knowledge of GxP principles is required.
- Experience with the following functions is preferred: clinical supply pack/label/distribution, clinical trial operations, project management, pharma/bio research and development, and inventory management.
- Experience with clinical supply demand management tools is preferred (e.g., tcVisualize, IVRS, SAP, OMP+).
- Demonstrable multitasking, project management, and execution skills.
- Good interpersonal skills, including communication, presentation, persuasion, and influence.
- Good organisational skills, including efficiency, punctuality, and collaboration in a team environment.
- Proficiency with computer skills, such as MS Office.
To Apply:
Please click on the Apply button. Please include a short note outlining why you are interested in the role and why you think you are suitable.
In case you have difficulty in applying or if you have any questions, please contact Luke Saner at +443300524502 or upload your CV on our website - www.Proclinical.com.
A full job description is available on request.
Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.
#LI-LS1
#TechOps
Related jobs
Highly Competitive
Caerdydd, Cymru
Are you passionate about diagnostic technology and helping laboratories maximise performance through expert product support and training?
Highly Competitive
London, England
Ready to lead global regulatory strategy and influence the development of innovative oncology therapies on a worldwide scale?
Highly Competitive
Burgess Hill, England
Join a forward-thinking analytics team where your insights will drive smarter decisions, stronger customer experiences, and market growth.
€90000.00 - €100000.00 per annum
München (81249), Germany
Ready to shape market growth across Europe and influence the future direction of a leading organisation in a highly regulated industry?
Highly Competitive
Zürich, Switzerland
Are you a network and infrastructure expert ready to drive the delivery of secure, scalable IT and OT environments while shaping the future of complex, business-critical projects?
Highly Competitive
Milton Keynes, England
Keep the heartbeat of innovation running! Join our client in this Automation Engineer position and ensure cutting-edge pharma operations never miss a beat!
Highly Competitive
Burgess Hill, England
Proclinical is on the hunt for a bold, innovative professional whose ready to help push the boundaries of science and make a tangible difference in the world.
Highly Competitive
Fort Worth, USA
Are you a detail-driven accounting professional looking to make a tangible impact on financial reporting, compliance, and business performance?
US$80 - US$87 per hour
Orlando, USA
Are you ready to lead cutting-edge research projects that accelerate clinical breakthroughs in biotech?
£50000 - £65000 per annum
Glasgow, Scotland
What if your expertise could help unlock the potential of some of the most challenging drug targets, driving innovative therapies from concept to discovery?