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. This role will be fully on-site and is 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, and validation of bioassays and clinical samples. This is 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 in cell culture, qPCR, RNA/DNA extractions, ELISA, and cell-based assays.
* In-vivo work experience, ideally within oncology (e.g., 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. #J-18808-Ljbffr