Time for change – time for a new job! You are a clinical supplies project manager and looking for a new professional challenge? Then stop searching! We offer the job you are looking for: Our subsidiary GULP solution services offers a secure job, fair compensation and exciting new tasks at an attractive BioPharma company in Ludwigshafen. Apply online now! We welcome applications from all suitably qualified persons regardless of any disabilities.
Das dürfen Sie erwarten
* Attractive salary and long-term job security through group affiliation
* Contribution to company pension scheme after end of probationary period
* Extensive social benefits, including Christmas and vacation bonuses
* As a rule, a permanent employment contract
* Tailored further training opportunities and free language courses
* A wide range of employee benefits
Ihre Aufgaben
* Represent CDSM activities as a member of the Clinical Study Team
* Provide input to Clinical Study Teams to influence clinical protocol design to ensure most efficient utilization of supply chain resources
* Translate clinical study design into packaging and distribution design
* Identify, develop, communicate and track project timelines, activities, logistics, and milestones
* Develop protocol specific labeling compliant with applicable global regulations
* Coordinate with CDSM Materials Management to establish study specific distribution plans for shipment of packaged supplies
* Manage inventory of finished goods and ancillary supply through study completion
* Track retest dates and subsequent dating extensions of study medication
* Responsible for creating appropriate protocol specific manufacturing and packaging work orders in concert with QA, Analytical, and clinical team partners, ensuring timely availability of clinical supplies
* Forecast and coordinate the execution of required packaging jobs including retest expiry label updates
* Responsible for project management of IRT activities
* Provide input and recommendation to CSPMs/DSMs on project timing, resource requirements, and budget projections
* Successfully participate in Process Improvement Initiatives
* Partner with Clinical Statistics and CDSM
* Coordination staff to prepare appropriate protocol specific randomization code files and blind breaker envelopes, as required
* Participate in CDSM Knowledge Management Meetings and presents relevant topics on an ad hoc basis
* Proactively provide input on process improvement opportunities
* Maintain and adhere to applicable Corporate and Divisional Policies and procedures
* Participate in troubleshooting and resolving clinical supply related issues ensuring that project needs and priorities are understood by key team members
* Effectively utilize MS Project to manage key project activities
Unsere Anforderungen
* Bachelor’s degree or equivalent education with several years of experience, or Master’s degree or equivalent education with several years of experience
* Proficient with standard computer software
* Able to effectively manage multiple projects at one time
* Able to think and act with regard to multiple functions with exceptional follow-up skills
* Strong project management skills
* Proactive approach to problem solving, thinking outside of the box, and ability to identify creative solutions to unique problems
* Strong communication skills (both written and oral)
* Able to work independently or with a group