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Research Assistant - temp
SRG
London
On-site
GBP 80,000 - 100,000
Full time
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Job summary
An established industry player is seeking a Research Assistant to join their dynamic team. In this role, you will play a crucial part in sample processing and analysis, ensuring compliance with quality documentation and GCP standards. You will work flexibly across shifts, contributing to the maintenance of sample integrity and supporting senior staff in clinical study planning. This position offers an excellent opportunity to develop your skills in a vibrant laboratory environment, where your contributions will directly impact the success of clinical trials. If you are passionate about scientific research and eager to grow in your career, this role is perfect for you.
Qualifications
- 1st Degree in a scientific subject (2:1 or above preferable).
- Experience with RT-qPCR and cell-based assays is essential.
Responsibilities
- Perform sample processing and analysis according to project documentation.
- Assist in lab maintenance and ensure sample integrity.
Skills
Education
Job description
Research Assistant
Position Type
Permanent & Temporary
- Same shifts as lab technicians (7am to 3pm or 3pm to 11pm).
- Shifts between 7am to 11pm for permanent positions.
- Will work 5 days out of 7 in a week (including weekends sometimes - need to be flexible).
- Temporary will be 8am to 5pm.
Main Responsibilities
- Perform sample processing and analysis in accordance with project and quality documentation.
- Perform lab maintenance tasks and cleaning.
- Assist in maintaining sample integrity by following sample storage procedures.
- Follow all applicable Policies, Standard Operating Procedures (SOPs), Study documentation, GCP, and any other applicable guidelines.
- Work as a member of a team.
- Organise own time and resources in an optimal fashion, with some guidance.
- Proactively review the schedule and ensure that all assigned tasks are completed, flagging any issues to the Laboratory Operations Manager.
- Deliver GCP compliant study data for the samples being processed or assayed.
- Assist with storage and tracking of samples, developing an understanding of HTA legislation.
- Assist with production of sample kits and sample label production.
- Support senior members of staff in the planning and delivery of clinical studies.
Skills & Experiences
- 1st Degree in relevant scientific subject (2:1 or above preferable) or equivalent.
- RT-qPCR or Cell-based assay experience.
- Tissue culture experience.
- Previous experience working to GCP standards and MHRA standards in a clinical trial environment.
- Experience working within a CRO or pharmaceutical company.
- Experience working within a virology or biomedical lab.
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