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Logistics Manager / Clinical Project Manager

Employer
RBW Consulting
Location
Europe
Salary
70000 - 90000 Euros / Annum
Start date
13 Sep 2022
Closing date
13 Oct 2022

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Discipline
Operations, Logistics
Hours
Full Time
Contract Type
Permanent
Experience Level
Experienced (non-manager)

Job Details

Clinical Logistics Manager / Project Manager

I am currently recruiting for an innovative Pharmaceutical Company based across Europe. They pride themselves on their innovative and dedicated  approach to the life science sector to enable better quality of human life. They are a global company who employ over 12,000 people across 100 countries  The role is permanent and can be fully remote if preferred, occasional travel to Europe may be required. The role would suit an experienced Logistics professional with clinical experience or a clinical project manager who may be looking to transition into logistics / supply chain.

This role can be based in any country in Europe.

Objective

Centralise and manage all logistics and supply tasks in the operational management of biologics clinical development programs. Ensure efficient and high-quality drug and supply management, oversee clinical drug and supply logistics for all trials and to support the RMP and supply procurement process.

KEY RESPONSIBILITIES:

  • Create, review, and update the trial supply plans based on strategic elements/study forecasts, which ensures efficiency in terms of cost, feasibility, and overage. Coordinate the randomization, packaging, labelling and distribution of clinical supplies according to study supply plans. Management of temperature excursions, including interaction with site staff & technical development manager/QP for evaluation of the excursion's impact, release, quarantine or replacement of the supplies. Ensure that key study milestones are met; negotiate and communicate supply plan with timelines to internal and external partners. Participate and support in internal/external inspections and audits. Author and review relevant SOPs.

MINIMUM QUALIFICATION REQUIREMENTS:

  • University degree or equivalent

ADDITIONAL REQUIREMENTS:

  • Solid operational experience in Clinical Research for a minimum of 3 years on a global level. Excellent planning and organizational skills with strategic thinking. Proven track record of ICH-GCP training. Team player with solid project management skills to lead assigned clinical trials as a member of an international project team. Excellent computer skills. Excellent oral and written communication skills in English

 

 

To find out more about this fantastic opportunity or to discuss other open positions which may be of interest please contact Ashley Clarke on +44 (0) 1273 952 363 and send your CV through using the apply button on this page.

 

 

 

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