Study Manager - CRO
Do you want to work for an award winning Contract Research Organisation who provides Clinical and Pre-clinical Molecular Pathology services to progress drug development? If so this Study Manager opportunity might be of interest. This is a permanent, full time position based in Hereford.
This Study Manager role will give you the opportunity to:
* Be responsible for the technical conduct of a study in addition to the interpretation, analysis, documentation and reporting of results to the client.* Develop study plans, and ensure that the plan and any changes made are appropriate and compliant to regulatory guidelines.* Monitor the progress and status of designated studies.* Ensure that all data gathered from experiments and observations are accurately documented and maintained.* Engage in client calls and visits to discuss the appropriate studies and provide technical support during discussions.* To recognise and advise of any technical weaknesses, and support a programme which can drive development.
As a Scientific Manager our client is ideally looking for the following skills and experience:
* A degree in an appropriate scientific discipline preferably MSc or Phd* Previous study management experience* Proven practical experience of Histology and Immunochemistry techniques (manual and automated)* Experience/ knowledge of working within a regulatory environment* Ability to judge current procedures and identify process improvement opportunities in an objective manner.
What should you do next?
Apply today, or alternatively feel free to email firstname.lastname@example.org for further information on this position.
Unless otherwise stated, if applying for a job within the European Union, you must ensure that you are already authorised to work there. SRG Ltd acts as an Employment Business and an Employment Agency on behalf of our client in recruitment for this role.See more at: www.srgtalent.com/jobs
your application has been submitted