Bioanalytical Study Monitor

An exciting pharmaceutical manufacturing company, based in Kent, are looking for a Bioanalytical Study Monitor to join their team. They purely specialise in providing CRO oversight, project management and consultancy services in bioanalysis and biologistics for the life science sector.

The role

The role will include acting as an expert resource for clients for the oversight and management of operational aspects of Large Molecule Regulatory PK and ADA bioanalysis at CROs. You will also develop and operate communication strategies and activity reviews of the outsourced bioanalytical activities undertaken by selected providers

Requirements:

• Degree/ masters level equivalent in a chemistry / biochemistry / biological science or similar discipline
• 4+ years industry experience is required
• Knowledge and competencies in designing and operational execution of clinical and pre-clinical studies, toxicokinetic and pharmacokinetic analysis
• Knowledge and competencies in application and practice of bioanalysis within regulatory environments (GLP and GCP)

In return you will receive a competitive salary, a clear career development path and the opportunity to work in a dynamic and fast-paces environment.

If this sounds like the role for you, please apply now!