We are currently working with a forward-thinking and exciting biotech organisation that are currently looking for an experienced and specialised GCP Auditor to join their base in Paris, France.
This is an extremely exciting and unique role that requires a specific individual to assist in all aspects of the company's QA expansion and activities. The responsibilities are vast and requires someone that is extremely passionate about this particular area and who is looking to become fully integrated in this dynamic organisation.
As the successful person you will be working closely with the Head of QA, providing contributions at a senior level to help develop the team and continuing QA strategy, including training and development of practices and processes. You will have full working access with board members, senior leaders and other senior individuals within the QA strategy allowing the opportunity to encourage changes within that senior level. You will also be responsible for managing investigational sites, clinical study protocols and audits within data management focusing particularly across US and EU. These responsibilities are at the forefront of the position, however there is capacity to influence the scope of full responsibilities dependant on what the successful candidate can bring to the role.
If you are interested in this one off opportunity and have an innovative and creative personality please contact Phil Barrett for a full confidential discussion and further information - eval(unescape('%64%6f%63%75%6d%65%6e%74%2e%77%72%69%74%65%28%27%3c%61%20%68%72%65%66%3d%22%6d%61%69%6c%74%6f%3a%70%68%69%6c%40%73%74%65%6c%66%6f%78%75%6b%2e%63%6f%6d%22%3e%70%68%69%6c%40%73%74%65%6c%66%6f%78%75%6b%2e%63%6f%6d%3c%2f%61%3e%27%29%3b'))
Senior, GCP, Good Clinical Practice, Compliance, audit, auditor, CAPA, Europe, training, Clinical QA, CQA, Quality, Quality Assurance, HA, Health Authority, FDA, EMA, MHRA, QMS, Trackwise, Switzerland, Basel, Paris, France, Germany, UK, EU, US
Deadline: 27 December 2013