One of the leading global CROs is looking to recruit a Senior Compliance Associate to join the QA department in the UK.
You will be responsible for GCP and GLP audits, QA reviews and evaluations and writing of SOPs. You will also provide training of GCP and GLP regulations.
You will be required to provide input and assistance to Business Development for time and cost proposal development and provide project management oversight for compliance-related tasks and programs.
To be successful in this role you must have experience in a similar position in clinical research, regulatory affairs or a relevant healthcare research position. You must have relevant GLP and GCP audit work experience ideally gained in a CRO
You will be required to travel up to 40% of the time, and have the motivation and drive to work independently.
A competitive remuneration package is available, as well as the opportunity to work for this exciting, well respected CRO.
For more information, please email Kristina on kristina@seltekconsultants.co.uk
Please note that applying to this role only expresses interest. We will discuss the role and company with you in detail before we send your CV.
Job Ref: 8090
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