I am currently working with a very interesting and exciting pharmaceutical company, based in Paris, who are actively seeking a Head of Quality Assurance to join their team. The company are going through a period of expansion at present, and are ideally looking for an experienced Quality professional, with 10+ years of Quality experience, experience in the supervision of Clinical Studies, and also the inspections program, adhering to both FDA and EMA regulations.
Due to an internal move a unique opportunity has arisen for a Global Senior Director of Study Management to join my client a leading boutique pharmaceutical company with an impressive development pipeline. This role will be working office based on a permanent basis in my client's world class facilities in Switzerland. ...
David Maunsell at Skills Alliance has partnered with a blue-chip pharmaceutical company in their search for a Medical Advisor to work on a...
Vice President of Global Start-Up – Growing, Midsized CRO – Ohio / London / Scotland
Company:Meet Salary: 100,000+ Benefits: For full details of the excellent benefits package then please get in touch
Closing Date: 19 Mar 15
Currently experiencing a sustained period of growth, my client is looking for an experienced Start-up professional to join their team as a VP of Start-up. This role is perfect for an experienced candidate looking for a new challenge with the chance to make an indelible mark on the CRO’s direction and progression
Hydrogen Life Sciences has been requested to search and select a Senior Director of Regional Quality. This permanent/staff position is required for a global pharmaceutical company with offices in Switzerland. It is a Senior Director level position within the company and has direct and indirect reports.
The main purpose of this role is to provide expert leadership to the Quality Assurance organisations in Asia, Africa and the Middle East. ...
The successful candidate would be responsible for all biostatistical aspects of the project including hypothesis stating, statistical planning, analysis and reporting. Our client is looking for someone with extensive experience as statistician in the clinical development in either pharmaceutical industry or clinical research organizations.
A growing biotech company in Massachusetts is expanding its Regulatory team to support late phase clinical responsibilities. The individual will operate in a highly visible role and will develop regulatory strategies and manage high-quality submissions to regulatory agencies globally. Director and Associate Director Regulatory Affairs levels needed. Competitive salary, bonus, long term incentives and relocation included. ...
Qualified Person - 12 months contract - Various Locations (UK, Germany)
Senior Statistician Office Based - Basel, Switzerland Contract until the end of 2015 (possibility for further extension) Start date (Feb/March 2015) Excellent Daily Rate - dependent on experience (up to 1000 CHF / day)
Rheumatology, Clinical development Director Permanent position email@example.com Reporting to the Global Development Head you will lead global clinical development programs for phase I-III clinical trials. You will be responsible for clinical study concepts and scientific aspects of study protocols.
My client, a Large Global Pharmaceutical Company, is keen to recruit an Industry experienced Medic with strong background in Oncology Medical Affairs to act as Head of Medical Affairs for Oncology in the UK.
This is a prominent regulatory affairs consultancy are looking to hire a focused and motivated individual as a Regulatory CMC Biologics Consultant at their site in Surrey. While focusing solely in the healthcare sectors this a company that has an innovative and forward-thinking working environment. This is a 6 month contract role with the possibility of an extension. ...
An internationally known pharmaceutical company situated in the South East, England and operating in over 150 markets worldwide is looking to hire a Senior Regulatory Labelling Consultant. The company develops a broad range of products in pharmaceuticals, vaccines and consumer healthcare. This is a 6 month contract with the possibility of an extension. ...
Freelance Clinical Data Manager - 6 months - Munich, Germany
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