Research Scientist - Clinical Trials

TN United Kingdom; London; On-site; GBP 40,000 - 70,000; Full time

Job summary

An innovative firm is seeking a proactive Research Scientist to join their laboratory team in London. This role focuses on supporting clinical trial delivery and laboratory operations, providing opportunities to develop practical skills in sample processing, assay performance, and data analysis. The ideal candidate will have a strong background in virology or biomedical sciences, with experience in GCP/GLP standards. Join a dynamic team and contribute to impactful clinical research while working in a collaborative environment that values flexibility and learning.

Qualifications

• Minimum 3 years experience in GCP/GLP standards.
• Experience in virology or biomedical labs.

Responsibilities

• Perform sample processing and analysis independently.
• Ensure GCP-compliant data delivery and project documentation.
• Support senior staff in clinical project planning.

Skills

GCP/GLP Standards

Virology Techniques

Sample Processing

Data Analysis

Education

Degree in Relevant Scientific Field

Job description

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Research Scientist - Clinical Trials, London

Client: hVIVO

Location: London, United Kingdom

Job Category: Other

EU work permit required: Yes

Job Reference: f480273e42d5

Job Views: 20

Posted: 05.05.2025

Expiry Date: 19.06.2025

Job Description:

Overview

hVIVO is seeking a proactive and experienced Research Scientist (RS) to join our laboratory team at sites in E1 & E14. This key role supports lab operations and clinical trial delivery.

The laboratory handles sample processing and analysis for all clinical trials at hVIVO, employing techniques like Qualitative and Quantitative PCR, cell infectivity, serology assays, and multiplex viral detection. The division manages internal studies, clinical trials, standalone projects, assay development, validation, and collaborates with partners.

The RS will support clinical trial delivery within our Laboratory Operations Department, working alongside a diverse team including Research Assistants, specialists, and Senior Virologists.

This lab-focused role offers opportunities to develop practical skills, including sample processing, assay performance, and data analysis. It also involves leading projects as Study Lead (SL), managing resources, data review, sample logistics, documentation, and training, under senior guidance.

The position requires working flexible shifts, including evenings and weekends as needed.

The ideal candidate will have a virology/biomedical background, experience with GCP/GLP in CRO/pharma settings, a degree or higher, and hands-on virology techniques like tissue culture, infectivity assays, and qPCR. Proactivity, learning desire, and flexibility are essential.

Main Responsibilities:

• Perform sample processing and analysis independently per project and quality standards.
• Maintain current knowledge of virology assays.
• Recommend experimental approaches.
• Ensure sample integrity and proper storage.
• Follow policies, SOPs, study documentation, GCP, and other guidelines.
• Collaborate effectively within the team.
• Organize own time and resources efficiently.
• Review schedules proactively, report issues.
• Ensure GCP-compliant data delivery.
• Assist with sample storage, tracking, and understanding HTA legislation.
• Conduct projects per protocol and timeline, adhering to GCP standards.
• Develop project documentation and services per client needs.
• Support senior staff in clinical project planning and delivery.

Skills & Experiences:

• Minimum 3 years of experience working to GCP/GLP standards.
• Experience in CRO or pharmaceutical environments.
• Experience in virology or biomedical labs.
• Degree in relevant scientific field (2:1 or above preferred).

Desirable:

• Understanding of HTA regulations.
• Project management experience.
• Knowledge of clinical GCP project delivery.

Additional Notes:

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