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Location (Berkshire) within 20 miles; Sector: Biotech / Pharmaceuticals; Posted within: 8 weeks
 
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  • Responsible for Global Immigration compliance, tracking cases and visa expiries in partnership with our external vendors....
  • University/college degree (life science preferred) or certification in a related allied health profession from an appropriately accredited institution...
  • You can make a difference by helping to deliver life-saving and life-enhancing medicines to people around the world. Our commitment to this mission ha...
  • We are currently seeking a proactive, driven Project Manager with experience in Drug Safety to join our expanding Safety team in our Maidenhead office...
  • The primary activity of the SAS Programmer is to develop and review SAS® programs and output for the management and reporting of clinical trial data. ...
  • Manager GSS
    Biotech / Pharmaceuticals
  • Covance
  • Maidenhead, Berkshire
  • 02/05/12
  • Responsible for line management of GSS personnel: hiring, mentoring, performance management; ensuring understanding of project specific and GSS polici...
  • Project Manager
    Biotech / Pharmaceuticals
  • Covance
  • Maidenhead, Berkshire
  • 02/05/12
  • You can make a difference by helping to deliver life-saving and life-enhancing medicines to people around the world. Our commitment to this mission ha...
  • Our Consumer Healthcare manufacturing centre in Maidenhead is one of the most advanced operations of its kind in the world. Dedicated to the producti...
  • To provide Quality and compliance support to (manufacturing) Production Operations and key functional groups across the site ensuring regulatory, QMS ...
  • This role involves direct responsibility for ensuring complete, accurate and timely accounting, reporting and compliance for a number of European comp...
  • To develop, implement and be accountable for product marketing plans which optimise profitability, market share and revenue growth in the short and lo...
  • Responsible for the provision of medical affairs support to the sales, marketing and regulatory teams in OU UK & Ireland to ensure we meet/exceed our ...
  • Responsible for managing CPO regulatory approval and outreach programs. Engages in trust-based scientific discussion with regulatory officials, while ...
  • A forensic scientist with DNA specialisation and court experience as an expert witness. Responsible for high throughput reporting of NDNAD matches and...
  • Develop and implement the product safety strategy and overall risk/benefit assessment, Integrate, analyse and clinically interpret safety information...
  • The role will require you to be medically qualified having obtained a medical degree or PhD along with a minimum of 7 years progressive experience in ...
  • As the Global Auditor Manager you will be joining their global operational excellence team and you will focus on Quality engineering, Global audit man...
  • Manage assigned geographic territory with regard to sales activities, including: Generate product interest and lead generation by performing cold call...
  • The FSE will act as an essential interface between the field organization and internal support structure by providing timely onsite technical assistan...
  • Clinical Data Manager
    Biotech / Pharmaceuticals
  • Cmed (Clinical Research Services) Ltd
  • United Kingdom
  • 02/05/12
  • You will have strong organisation and communication skills and a thorough understanding of medical terminology, physiology, pharmacology and the drug ...
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