CK Group are recruiting for a Development Scientist with clinical sample bioassay validation expertise, to join a growing biotechnology company on a permanent basis to be based in Oxford.
Skills, Experience, Qualifications, If you have the right match for this opportunity, then make sure to apply today.
This role will be fully on-site and a great opportunity to take responsibility in a fast-paced environment, working within an interdisciplinary team, to develop new cancer treatments.
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 119 690 in all correspondence.
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