Drug Supply Co-ordinator

vor 2 Wochen

Home Office, Schweiz Thermo Fisher Scientific Vollzeit

**Drug Supply Coordinator**

**Remote**

As part of the Thermo Fisher Scientific team, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world’s toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer.

**Your Key Responsibilities**
- Handle inventory and shipment delivery of clinical trial materials and work with appropriate parties to address any issues which might impact the timely delivery of supplies to distribution depots and clinical trial sites
- Produce manual or IRT reports and metrics as agreed for study tracking
- Summarize data and make recommendations for action relative to the clinical supply chain and packaging plans
- Work with both internal and client Project teams to ensure consistent communication of material supply status and identify potential risks and proactively raise issues
- Support expiry date management by identifying inventory to be extended, supporting the extension process and updating IRT status as appropriate
- Monitor and handle temperature excursions of clinical trial materials according to client expectations; ensuring that all personnel are aware and take appropriate measures disposition or replace impacted drugs
- Coordinate return, destruction, complete reconciliation and file archiving of drugs on assigned studies
- Ensure Budget Tracking with Monthly Billing and follow-up
- Identify and/or recommend process improvements based on understanding of clinical trial supply chain management standard methodology principles and appropriately documents and revise or develop associated training materials
- Act as back up for other members of the supply chain team
- Stay on top of relevant cGMPs, GCPs, and other regulatory requirements and ensures study management activities are aligned
- Conduct activities in a safe and efficient manner
- Demonstrate and promote company vision
- Other duties may be assigned to meet the needs of the business

**Education**
- Bachelor’s degree or equivalent in science-related field required (equivalent work experience may be considered)

**Experience**
- Knowledge in clinical trial supply chain management methodologies
- Experience working in GxP regulated environment
- Excellent digital literacy, including high proficiency with Microsoft Suite including Excel, Word and MS Project as well as the Office 365 environment.

**Knowledge, Skills, Abilities**
- Outstanding teamwork
- Strong interpersonal and presentation skills, both verbally and written.
- Accuracy and attentiveness to details
- Ability to independently balance priorities and workday in a remote setting
- Strong project and self management skills
- Ability to identify problems and work toward a solution

Our Mission is to enable our customers to make the world healthier, cleaner and safer. Watch as our colleagues explain 5 reasons to work with us. As one team of 100,000+ colleagues, we share a common set of values - Integrity, Intensity, Innovation and Involvement - working together to accelerate research, solve complex scientific challenges, drive technological innovation and support patients in need.
**_ #StartYourStory at Thermo Fisher Scientific_**, where diverse experiences, backgrounds and perspectives are valued.

**_Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status._**
- Accessibility/Disability Access_

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