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- 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.
- 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.
- Other info: Collaborate with experts and lead projects in a supportive team.
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.
- 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.
- Understanding of HTA regulations.
- Project management experience.
- Understanding of the clinical aspects of delivering GCP projects.
Research Scientist - Clinical Trials in London employer: hVIVO
Contact Detail:
hVIVO Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Research Scientist - Clinical Trials in London
✨Tip Number 1
Network like a pro! Reach out to professionals in the virology and biomedical fields on LinkedIn. Join relevant groups, attend webinars, and don’t be shy about asking for informational interviews. We all know that sometimes it’s not just what you know, but who you know!
✨Tip Number 2
Prepare for those interviews by brushing up on your technical skills and knowledge of GCP/GLP standards. We recommend practising common interview questions related to clinical trials and virology techniques. Show them you’re not just a candidate, but the candidate they’ve been looking for!
✨Tip Number 3
Don’t forget to showcase your hands-on experience! Whether it’s through a portfolio or during interviews, highlight your practical lab skills and any projects you’ve led. We want to see how you can contribute to the team at hVIVO!
✨Tip Number 4
Apply directly through our website! It’s the best way to ensure your application gets seen. Plus, it shows you’re genuinely interested in joining our team. Let’s get you started on this exciting journey together!
We think you need these skills to ace Research Scientist - Clinical Trials in London
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the Research Scientist role. Highlight your experience with virology techniques and any relevant projects you've led. We want to see how your background fits with our lab operations!
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Share your passion for clinical trials and how your skills align with our needs. Don’t forget to mention your flexibility and eagerness to learn – we love proactive candidates!
Showcase Relevant Experience: When detailing your experience, focus on your hands-on work with GCP/GLP standards and any specific assays you’ve performed. We’re looking for someone who can hit the ground running in our lab, so make it clear how you can contribute!
Apply Through Our Website: We encourage you to apply directly through our website. It’s the best way to ensure your application gets into the right hands. Plus, it shows us you’re serious about joining our team at hVIVO!
How to prepare for a job interview at hVIVO
✨Know Your Techniques
Make sure you brush up on the key virology techniques mentioned in the job description, like PCR and cell infectivity assays. Be ready to discuss your hands-on experience with these methods and how you've applied them in previous roles.
✨Show Your Proactivity
hVIVO is looking for a proactive individual, so come prepared with examples of how you've taken initiative in past projects. Think about times when you identified a problem and took steps to solve it without being asked.
✨Understand GCP/GLP Standards
Since the role requires working to GCP/GLP standards, be sure to familiarise yourself with these guidelines. You might be asked how you've adhered to these standards in your previous work, so have specific examples ready.
✨Teamwork is Key
The position involves working closely with a diverse team, so be prepared to discuss your teamwork skills. Share experiences where you collaborated effectively with others, especially in a lab setting, and how you contributed to the success of a project.
