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The Role:
Contributing to strategic R&D goals, the successful candidate must be proactive with experience working to GCLP/GCP as you will be supporting and performing in the development, qualification, validation of bioassays and clinical samples. An exciting time to join a growing biotech and be part of a dynamic team contributing to the translation of early stage oncolytic virus products through to clinical development.
Your responsibilities will include:
- Performing bioassay development, validation experiments and patient sample analysis under GCLP.
- Management and performance of sample processing.
- Timely delivery of biomarker lab data for clinical trials.
Your Background:
- Degree qualified (MSc/ PhD) with industry experience in clinical bioassay validation (essential), analysis, and clinical sample management in the industry setting.
- Up-to date GCLP certifications.
- Hands on sample management expertise.
- Technical experience on cell culture, qPCR, RNA/DNA extractions, ELISA and cell-based assays.
- In-vivo work experience, ideally within oncology (eg. mice bearing human tumours) and working with patient samples (DESIRABLE).
Benefits:
- Bonus.
- Pension.
- Private Medical Insurance.
- Flexible working hours.
Apply:
It is essential that applicants hold entitlement to work in the UK. Please quote job reference (Apply online only) in all correspondence.
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