Precision for Medicine is hiring a Research Assistant I to join our well-established scientific team in Royston UK who have been supporting biopharmaceutical research for over 25 years.
The biopharmaceutical industry continues to undergo transformational change with new and exciting developments in biotherapeutics, immune oncology, companion diagnostics and personalised healthcare. As a global leader in the provision of clinical biomarker-based solutions to the biopharmaceutical industry, we are developing and expanding our research and clinical services in the UK to serve this expanding market and are looking for a dynamic, self-motivated Research Assistant I to join the team and contribute to the growth of the company.
The Research Assistant role in our genomics team will be responsible for supporting the Senior Scientist with qRT-PCR projects, conducting meticulous qRT-PCR-based lab work to enable delivery of high quality data. The successful candidate should have around 1-2 years’ relevant laboratory experience, ideally gained working in a commercial, regulated laboratory (GLP and/or GCLP) or clinical diagnostic environment.
Duties and Responsibilities:
1. Provide high quality practical support for genomics projects by performing experimental work and assisting with the analysis, interpretation and reporting of experimental data.
2. Responsible for sample management, from sample receipt and accessioning, to DNA/RNA extraction and quantification, data QC.
3. Execution of qRT-PCR and other PCR based studies, working to established SOPs.
4. Production of accurate, high-quality data.
5. Assist in the development of new methodologies or evaluation of new technologies as required.
6. Management of critical reagents.
7. Provide routine maintenance and calibration of genomics equipment.
8. Write laboratory documents including risk assessments, COSHH assessments, and SOPs.
9. Maintain and support safe lab practices and environment.
10. Generate, protect, and maintain raw data, analysed, reported data and associated metadata, including sample, reagent and methodology details.
11. Maintain accurate, up to date records (lab book, internal databases, and timesheets).
Regulatory:
1. Comply with all quality management, regulatory compliance, and project management processes (GxP, HTA, H&S).
2. Work to the current Good Clinical Practice for Laboratories (GCLP) standards and maintain appropriate training and qualifications.
Other:
1. Participate in on-call rota for out-of-hours work.
2. Actively participate in performance review and personal development processes required.
3. Contribute to other laboratory teams and projects as required.
Qualifications and Experience:
1. Level 4 qualification, HNC in Biological sciences (or other relevant life science subject) or equivalent.
2. 1-2 years of laboratory experience, ideally with qRT-PCR assay execution.
Preferred:
1. Degree in Biological sciences (or other relevant life science subject).
2. Experience of working in a regulated environment such as GxP and the Human Tissue Act.
3. Proof of vaccination against Hepatitis B (vaccination can be arranged).
4. Excellent communication skills both verbal and written.
5. IT skills, particularly Microsoft tools. Experience working with sample management databases would be an advantage.
6. Ability to lift and carry between 1-7kg.
Personal Attributes:
1. Team player with strong interpersonal skills, but able to work on own initiative.
2. Keen to learn and develop.
3. Excellent attention to detail.
4. Organised and tidy.
5. Ability to cope under pressure.
6. Good with time keeping.
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