Clinical Trial Supply Manager - Basel, Schweiz - CTC Resourcing Solutions

CTC Resourcing Solutions

Geprüftes Unternehmen

Basel, Schweiz

vor 2 Wochen

Geschrieben von:

Lena Schneider

beBee Recruiter

Beschreibung

The Life Science Career Network
Our client is a biotechnology company, developing next generation cancer vaccines based on viral vector technologies.

We are currently looking for a
Clinical Trial Supply Manager for a contract role, fully remote, for applicants living in Switzerland.

Your responsibilities include conducting and overseeing all supply chain activities and document design (labelling) according to SOPs, cGCP, cGMP, and all applicable regulations.

Main Responsibilities:

Liaising with and overseeing Clinical vendors for management of clinical supplies in compliance with appropriate regulations
Working with Clinical Trial Managers to formulate and prioritize short

- and long-term objectives with respect to clinical supplies and implementing strategies

Ensuring clinical trial supplies are ordered, managed, and delivered within agreed budget and timelines
Working with Clinical Operations team in preparing and modifying timelines for clinical trial supply chain activities
Supporting the development and implementation of processes and standards and providing a source of process improvement targets and ideas.
Maintaining relationships with pharmaceutical partners and their CTS groups
Working with Logistics / Supply Chain and QA team in developing and implementing process improvement plans and structure in relation to clinical trial supply management
Ensuring appropriate, comprehensive and professional communications both internally and externally
Participating in Clinical Study Team meetings to provide Clinical Trial Supply status updates and expert advice

Qualifications and Experience:

Relevant working/residency permit or Swiss/EU-Citizenship required
Relevant university degree or educational experience with 3+ years pharmaceutical industry experience within clinical operations
Management experience in global clinical trial supplies and associated regulatory requirements
Experience in coordinating clinical trial materials, labelling, packaging and distribution to trial centers
Knowledge of the drug development process and clinical development planning
Successful experience in coordinating internal and external resources and in working with pharmaceutical partners
Direct handson experience in managing highquality successful clinical supply chain
Clinical and operational knowledge, with continuous expansion and learning ability
Fluent in English, Italian is a plus