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Clinical Supply Manager - Basel



Business Type: Pharmaceutical Company
Job Type: Clinical Supplies
Job Level: Experienced (non manager)
Position: Full Time
Location: Switzerland
Reference: DW.26564432894392008
Closing Date: 10/08/20
Job Details:

On behalf of one of the top 3 Pharma companies who are looking for a Clinical Supply Manager, on a contract basis for at least 12 months to be based in Basel. This is a chance to be a part of one of the largest pharmaceutical companies in the world, where extensions are expected allowing you to gain exposure with a reputable name and ultimately build further value for your profile.

Job Title: Clinical Trial Supply Manager

Role Purpose

GCS Clinical Trial Supply Manager (CTSM) defines and executes an optimal clinical trial supply strategy for a clinical trial including effective risk management to ensure supply continuity to patients.
The CTSM is the GCS single point of contact at trial level for the integrated Clinical Trial Team (iCTT). Is responsible for clinical trial supply deliverables within GCS and all other relevant associated sub-functions, maintaining Quality and Compliance through all activities.
Has operational end to end responsibility for assigned activity. Leads and manages all project and local network activities and participates in cross-functional teams.

Key Performance Indicators (Indicate how performance for this job is measured)

1. Accountability for quality, quantity and timelines for all assigned tasks/projects
2. GMP Compliance (number of deviations, technical issues, audit / inspection findings)
3. Adherence to standards and Values & Behaviors, in particular, quality, ethical, health, safety, and environment standards (HSE), and information security standards (ISEC).
4. Unit KPIs. Cross-functional KPIs (if applicable)

Languages: Fluent in English

Experience/Professional requirement:
1. at least 5 years of practical experience in chemical / pharmaceutical Industry, 3 years of experience in field of expertise
2. Good expertise in related field.
3. Good knowledge about the Drug Development process
4. Basic project management , good organization and planning skills
5. Knowledge of relevant regulations (e.g. GMP, HSE etc.)

Call me Daniel Watson at NonStop Recruitment now for a confidential conversation. Contact me on D.Watson@nonstopconsulting.com or +41 435 080 817, please send your CV in word format OR if this does not sound like the opportunity for you, but you are a Contract professional within the pharmaceutical, medical device or biotech industry, please feel free to get in touch, to see other opportunities we may have within this field.

NonStop is one of the largest and fastest growing specialised life sciences recruitment companies in Europe. We are proud members of the APSCo life sciences group who ensure we meet the highest quality standards within the recruitment industry. Our offices are located in the UK, Switzerland and the Czech Republic and we hold labour leasing licences across Europe. Please visit our website for a full list of the niche markets we cover.



Posted: 03/08/2020 | NPJ Ref: 257077
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