Research Assistant - FluCamp Clinical Trials

Overview

hVIVO are currently looking for a Research Assistant (RA) to join our laboratory team at our site in Canary Wharf, east London. The RA role is a key role within lab operations assisting in the delivery of clinical trials processing samples, performing assays and data analysis.

The hVIVO Lab function supports the delivery of clinical trials for external and internal clients by performing sample processing and analytical techniques including Qualitative and Quantitative PCR, cell infectivity, neutralising antibody and serology assays, and multiplex viral detection assays. This is done for clinical trials performed at hVIVO and for external trials. The Lab also performs bespoke assay development and validation work and collaborates with strategic partners.

The role involves working to a flexible shift pattern including working evenings and weekends as required to deliver the operational plan.

The ideal candidate will have a virology/microbiology/biomedical background working to Good Clinical Practice (GCP) as part of a Clinical Research Organisation (CRO) or pharmaceutical company. They will be degree educated and have hands-on experience of key virology techniques including tissue culture, cell-based infectivity assays and qPCR. Be a proactive individual with a desire to learn and progress in a GCP environment. Be flexible with working patterns to suit the needs of the business.

This is a full-time position (37.5 hours per week) working shifts across Monday - Sunday. Shift Patterns are as follows:

1. 07:00 - 15:00
2. 09:00 - 17:00
3. 15:00 - 23:00

Main Responsibilities

• Performing 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 the applicable Policies, Standard Operating Procedures (SOPs), Study documentation and GCP and any other applicable guidelines;
• Work as a member of a team;
• Responsible for organising 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;
• Responsible for the delivery of GCP compliant study data for the samples being processed or assayed;
• Assist with storage and tracking of samples, develop 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;
• Microbiology 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;