One of the leading global CROs is looking to recruit a Senior Compliance Associate to join their offices in the UK.
It's a rare opportunity in QA for someone who wants to acquire the experience required to become a QA Manager in the near future
You will be responsible for GCP audits, QA reviews and evaluations and writing of SOPs. You will also provide training to clinical research staff on GCP 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 audit work experience ideally gained in a CRO and strong working experience of GLP, GMP and GCP Audits
You will be required to travel up to 40% of the time, and have the motivation and drive to work independently.
Job Ref: 8061
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