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Clinical Data Analyst/Statistician/Medical Writer – Permanent – Basel, SwitzerlandThis is an exciting opportunity for an experienced Clinical Data Analyst/Statistician/Medical Writer to expand their knowledge and develop their career in a fast growing Swiss pharmaceutical company. They are looking for the right person to join a motivated and dedicated team.Requirements / Experience
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The Statistician is responsible for ensuring that CLIENT’s statistical activities are conducted in accordance with the clinical trials legislation and guidelines. The Statistician is a member of the Biometrics Team and will coordinate and manage the deliverables involved in multiple clinical studies from study concept through to publication.
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PPD is a leading global contract research organization providing drug discovery, development and lifecycle management services. Our clients and partners include pharmaceutical, biotechnology, medical device, academic and government organizations. ...
- Clinical Data Manager - Specialist CRO (Clinical Imaging) - London
A rapidly growing and ambitious CRO, specialist in the field of Imaging Services is looking to appoint a Clinical Data Manager to manage data in raw form of images and scans and manage its conversion into Clinical Trial Data and reporting to the sponsors.
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A Clinical Scientist is required to join a fast growing specialist biotech company developing an exciting range of synthetic peptide immunoregulatory epitope products.
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- Associate Director - Clinical Development - International Pharma - £80k-£100k, Car + Car Allowance, 15% bonus, +more
An International Pharmaceutical company is looking to appoint an Associate Director in Clinical Development to be based in Middlesex. A well-remunerated and crucial appointment which will involve being responsible for the Medical Direction and Clinical Strategy across Gastroenterology Studies, Phase III to IV.
- Regulatory Affairs Officer - Labelling
Our client, a fast growing British pharmaceutical company, is seeking a dedicated Regulatory Officer with labelling experience to join the expanding team, initially on a 12 month contract, based in Bedfordshire. As Regulatory Officer, you will report to the Regulatory Manager and join a team that is committed to nuturing its own talent, actively encouraging development and providing training.
- Senior Regulatory Affairs Officer/Senior Regulatory Affairs Associate
I am currently seeking a Senior Regulatory Affairs Officer to join a global specialist Pharmaceutical & Medical Device Company in a brand new state of the art facility based in Maidenhead. 12 Month FTC offering a salary of up to £45,000 + bonus + benefits