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Senior Management
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Head of Bulk Manufacturing
Looking for an experienced Manufacturing Leader to join one of the top pharmaceutical companies as Associate Director Bulk Manufacturing, Berlin area
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Associate Director Process Engineer - Pharma - North Germany
Associate Director Process Engineer for Pharmaceutical Production - CapEx Projects
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Senior Manager; Observational Research & Programmer
Senior Manager; Observational Researcher & Programmer within Epidemiology. Location: Homebased/ Stockley Park Client: research-based biopharmaceu...
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Director / Senior – Biomarker Strategy – Metabolic / Metabolism
We have an exciting opportunity available as a Senior Director/ Director at a growing biotechnology company responsible for building a new team and...
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Senior Statistician
Are you passionate about research and development but also keen to maintain a work life balance? Then we want to speak with you!
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Vice President, R&D - Medical Devices
Vice President - R&D Medical DevicesAuckland, NZExcellent Remuneration Package
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Head of Pharmaceutical Technology Programme
International Pharmaceutical Manufacturer requires an experienced Technology Programme Head
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Associate Director (Market Research)
Hobson Prior are working with an innovative pharmaceutical organisation who focus on providing research intelligence and strategic recommendations.
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Senior Regulatory Affairs Consultant - NEW ROLE- Do you have European Product launch experience?
To apply for this regulatory affairs role please call Julie Cooper on 07951 082482 or email your CV in confidence to :julie@mosaicrecruitment
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Senior Research Executive
Hobson Prior are working with an innovative pharmaceutical organisation who focus on providing research intelligence and strategic recommendations.
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Global Manager - Health Economics and Outcomes Research
heor senior manager, germany, Senior HEOR, Health Economics
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HEOR - Global Manager - 3 years experience plus
heor senior manager, germany, Senior HEOR, Health Economics
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Director of Clinical Development- Oncolytic Viruses
Join a dynamic pharma company and work with oncological viruses to help treat and cure cancers.
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Clinical Associate Director
Key responsibilities Design, implementation, monitoring, analysis, and reporting of global clinical studies and act as a clinical representative ...
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CMC Consultant
Tasks & Responsibilities: · Provide advice to clients on quality aspects of drug development and regulatory requirements, in close collaboration wi...
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CAPA Quality Engineer
Job Description The Quality Engineer (m/w/d) - CAPA drives activities and procedures associated with CAPA and other Quality tasks concerning compan...
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Medical Writer
The Medical Writer is responsible for creation of medical and scientific documents and the factual and formally correct display of scientific resul...
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RA Specialist: Medical Devices
A thrilling opportunity has arisen for a Senior Regulatory Affairs Specialist to join a forward thinking Medical Device company who are pioneering ...