Clinical Supply Manager (m/f/d)

REFERENCE NUMBER:

508297/1

MY DUTIES:

- Represent Global Clinical Supply as a core member in the integrated Clinical Trial Team (iCTT); defines and advises the iCTT on the optimal clinical trial supply strategy in terms of, but not limited to, packaging design, technical and timeline feasibility, efficiency and risk management
- Review overall clinical trial protocol/protocol amendments, provides inputs to develop optimal packaging design, clinical trial supply design and visit schedule
- Create and maintain complete and accurate clinical supply demand for assigned study in alignment with protocol requirements, key study parameters and milestones, patient projections, with appropriate overage and by using defined processes and systems
- Create and drives finalization of the packaging design (Clinical Packaging Request) and a comprehensive label strategy for all participating countries in the clinical trial
- Define clinical supply parameters for the company set up and initiates subsequent updates throughout the duration of the clinical trial
- Develop and execute a trial-level project plan together with all other relevant roles
- Identify, assess and proactively communicate supply risks to all relevant stakeholders along with appropriate mitigation strategies to ensure supply continuity
- Collaborates with all relevant line function partners for country submission and approval timelines (including INDIMPD amendment) to develop optimal supply strategy
- Generates optimal distribution plans for investigational medicinal products (IMPs), jointly with partner functions.Triggers and tracks shipments of IMPs from central depot to regional hubs and local depots
- Develop, maintain and execute an optimal resupply strategy with proactive planning, appropriate lead-time and replenishment quantities to ensure compliance and continuity of clinical supplies, including proactive expiry management of clinical supplies

MY QUALIFICATIONS:

- University degree in science, engineering or equivalent, fluent in English 
- Profound practical experience in chemical / pharmaceutical industry,profound experience in field of expertise
- You have experience in Clinical Supply Chain working in a clinical trial team linked to packaging design, technical and timeline and risk management
- Good knowledge about the Drug Development process
- Basic project management , good organization and planning skills
- Knowledge of relevant regulations (e.g. GMP, HSE etc.)
- Demonstrates problem-solving and idea generation skills, good presentation skills and fundamental Leadership skills

MY BENEFITS:

- Well known pharmaceutical industry 
- Option to extend the contract for another year or to be internalized 

ABOUT HAYS:

With over 15 years of experience in the pharmaceutical industry, biotechnology and medical engineering, we know the key contacts at companies that are recruiting for challenging jobs with real potential. The current high demand for staff has opened up exciting opportunities for dedicated professionals looking to develop themselves professionally and to further their careers. As recruitment specialists with an international network of contacts, we can offer you decisive advantages – all completely free of charge. Register with us and reap the benefits of job offers that are both interesting and relevant to your skills and experience.

MY CONTACT AT HAYS:

My contact person
Emina Mustafic

Reference number
508297/1

Contact
E-Mail: [email protected]