Research Scientist - Clinical Trials in London

Research Scientist - Clinical Trials in London

London Full-Time 36000 - 60000 £ / year (est.) No working from home possible
hVIVO

At a Glance

  • Tasks: Join our lab team to process samples and analyse data for clinical trials.
  • Company: hVIVO, a leading company in clinical trial research.
  • Benefits: Gain hands-on experience, flexible shifts, and opportunities for career growth.
  • Other info: Collaborate with experts and lead projects in a supportive team.
  • Why this job: Make a real impact in virology while developing your skills in a dynamic environment.
  • Qualifications: Degree in a relevant scientific field and experience in GCP/GLP standards.

The predicted salary is between 36000 - 60000 £ per year.

hVIVO are currently looking for a proactive and experienced Research Scientist (RS) to join our laboratory team across our sites in E1 & E14. The RS position is a key role within lab operations and is critical in assisting in the delivery of clinical trials. The hVIVO Laboratory function undertakes the sample processing and analysis for all clinical trials conducted at hVIVO. The RS position exposes applicants to a range of practical techniques including Qualitative and Quantitative PCR, cell infectivity, neutralising antibody, serology assays and multiplex viral detection assays. The laboratory division has a diverse work stream including internal studies, clinical trials and standalone projects. The laboratory division also performs bespoke assay development and validation work and collaborates with strategic partners.

The RS will work as part of our Laboratory Operations Department supporting the delivery of clinical trials. The wider team includes individuals with a wide range of experience including Research Assistants, specialists in specific areas and Senior Virologists. The RS role is a lab focused position with room to develop and refine practical laboratory skills. The day to day work includes processing samples, performing assays and analysing data. The role offers significant growth as the position also requires leading projects (internal and external) by acting as Study Lead (SL). The SL is responsible for the smooth day to day running of the analytical phase of clinical trials performed at hVIVO, working under the guidance of a senior scientist. This gives applicants exposure to the responsibility and skills required for future project management positions. The SL role includes study resource management, matrix management of colleagues, and responsibility for data review and quality, sample logistics, document writing and delivery of training.

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

Main Responsibilities
  • Performing sample processing and analysis in accordance with project and quality documentation, with a high degree of independence.
  • Have a good working knowledge of current assays used in the field of virology; Make recommendations for the performance of scientific experiments in project areas.
  • 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.
  • Conduct projects according to the agreed protocol and timeline in line with GCP standards.
  • Develop project documentation and services, in line with client requirements.
  • Support senior members of staff in the planning and delivery of clinical projects.
Skills & Experiences
  • Previous experience working to GCP / GLP standards, minimum 3 years full time.
  • Experience working within a CRO or pharmaceutical company.
  • Experience working within a virology or biomedical lab.
  • 1st Degree in relevant scientific subject (2:1 or above preferable) or equivalent.
Desirable
  • Understanding of HTA regulations.
  • Project management experience.
  • Understanding of the clinical aspects of delivering GCP projects.

Research Scientist - Clinical Trials in London employer: hVIVO

hVIVO is an exceptional employer that fosters a collaborative and innovative work culture, providing Research Scientists with the opportunity to engage in cutting-edge clinical trials while developing their practical laboratory skills. Located in the vibrant areas of E1 and E14, employees benefit from a diverse range of projects and the chance to lead significant studies, ensuring ample opportunities for professional growth and advancement in a supportive environment. With a commitment to quality and excellence, hVIVO empowers its team members to thrive in their careers while contributing to impactful scientific research.

hVIVO

Contact Details:

hVIVO Recruitment Team

StudySmarter Expert Advice🤫

We think this is how you could land Research Scientist - Clinical Trials in London

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We think you need these skills to ace Research Scientist - Clinical Trials in London

Qualitative and Quantitative PCR
Cell Infectivity Assays
Neutralising Antibody Assays
Serology Assays
Multiplex Viral Detection Assays
Sample Processing and Analysis
GCP / GLP Compliance

Some tips for your application 🫡

Show Off Your Lab Skills:In the biotechnology field, it's super important to highlight your lab experience in your CV. Be sure to mention specific techniques or instruments you've mastered (think PCR, gel electrophoresis, etc.) and any relevant projects you've worked on. This will show hVIVO that you have the hands-on skills they need.

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Craft a Compelling Cover Letter:Since this is a full-time role, your cover letter should reflect not only your passion for biotechnology but also your long-term career ambitions. Share why you're excited about the work that hVIVO does and how you envision contributing to their goals. This shows that you’re not just looking for any job, but you're genuinely invested in this opportunity.

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How to prepare for a job interview at hVIVO

Brush Up on Lab Techniques

Since you're eyeing a full-time gig in biotechnology, make sure you're well-versed in the lab techniques relevant to the role. Be ready to talk about PCR, CRISPR, or any specific methods mentioned in the job description at hVIVO. You might even be asked to demonstrate your understanding of these processes.

Know Your Bioinformatics Tools

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