QC Analyst

Role Overview

Are you an experienced IT Business Analyst with a passion for driving meaningful change? This is your opportunity to make an impact by acting as the vital bridge between business needs and IT solutions for our client. You’ll play a central role in shaping future business processes, aligning IT capabilities with organisational objectives, and becoming a trusted advisor within a forward-thinking team. If you’re looking for a role where your expertise genuinely moves the needle, this position is for you.

About Our Client

Our client operates within a dynamic and evolving environment, working to deliver innovative solutions and improve core business systems. They are committed to fostering growth, collaboration, and a culture of innovation, making this a fantastic opportunity to join a team that values expertise and supports professional development.

About the Role

• Collaborate with stakeholders to analyse, define, and document business processes, driving alignment with IT capabilities.

• Lead workshops and foster collaboration to ensure seamless delivery and stakeholder buy-in across global networks.

• Drive organisational change by taking ownership of project risks, priorities, and testing efforts, ensuring exceptional delivery outcomes.

• Provide expertise in business solutions and contribute to continuous improvement efforts, shaping the organisation’s future state vision.

• Adhere to industry-standard policies and procedures while developing an understanding of data systems and architecture.

Skills

• Business Analysis Excellence: Skilled at uncovering requirements and turning them into actionable IT solutions.

• Stakeholder Management: Confident in building trust, leading discussions, and ensuring team alignment to achieve shared goals.

• Risk & Change Management: Expertise in identifying risks, testing changes, and maintaining smooth project delivery.

Next Steps

If you’re ready to bring your IT business analysis expertise to a role that offers both challenge and opportunity, we’d love to hear from you. Apply now to start a conversation about this exciting next step in your career.

Laboratory Technician

Reporting to: Operations Manager

Site: 100% On-site

Hours: 37.5 per week

Are you looking to build a career within a scientific and laboratory environment?

We're looking for a motivated and hands-on individual to join a growing organisation that is passionate about developing people and providing long-term career opportunities. This role offers excellent exposure to laboratory operations and is ideal for someone who is eager to learn, adaptable, and enjoys working in a fast-paced, practical environment.

Previous laboratory experience can be beneficial, but attitude, reliability, and a willingness to get stuck in are far more important. Full training will be provided, making this an excellent opportunity for someone looking to develop a career in science, laboratory operations, or the life sciences sector.

Key Responsibilities

Support the day-to-day running of laboratory and operational facilities.

Maintain a clean, organised, and safe working environment.

Assist with the receipt, logging, storage, and movement of samples and laboratory materials.

Support inventory management and stock control activities.

Help monitor and maintain laboratory equipment and site systems.

Assist with routine facility checks and operational tasks.

Maintain accurate records and documentation.

Support purchasing and general operational activities.

Follow quality, safety, and company procedures at all times.

Work collaboratively with colleagues across laboratory and operations teams.

What We're Looking For

Hard-working, reliable, and proactive attitude.

Willingness to learn new skills and take on responsibility.

Hands-on approach and ability to work in a practical environment.

Strong attention to detail and organisational skills.

Good communication skills and ability to work as part of a team.

Adaptable and comfortable working across a variety of tasks.

Basic IT skills.

Desirable

Previous experience in a laboratory, warehouse, manufacturing, engineering, logistics, or operational environment.

An interest in science, healthcare, or laboratory-based work.

Exposure to regulated or quality-driven environments.

What's on Offer?

Structured training and development.

Opportunity to build a long-term career within a scientific environment.

Exposure to laboratory operations and regulated processes.

Supportive team culture with genuine opportunities for progression.

A varied and hands-on role where no two days are the same.

Laboratory, technician, Science, samples, Research, Pharmaceutical, Biotechnology, Documentation, Life Sciences

Immunohistochemistry Scientist

📍 On-Site | Full-Time, 37.5 hours per week
🧬 Preclinical & Translational Research

Key Responsibilities

• Design, develop and optimise automated IHC assays using relevant tissues, controls, and reagents.

• Independently design and execute experiments, analyse data, and communicate findings.

• Generate high-quality scientific data and provide expert technical input across client projects.

• Troubleshoot assay performance and resolve scientific challenges efficiently.

• Prepare high-quality project proposals, study reports, and scientific documentation.

• Manage project timelines and contribute to successful client delivery.

About You

Essential Requirements

• BSc degree in Biology, Biomedical Sciences, Life Sciences, or a related discipline.

• Minimum 3-4 years' work experience developing, analysing, and reporting high-quality research data using automated IHC platforms.

• Proven ability to analyse scientific data and produce high-quality reports.

• Excellent organisational skills and attention to detail.

• Strong communication skills with the ability to work effectively across teams.

• Full right to work in UK

Desirable Experience

• Experience within a CRO, contract research, or biopharmaceutical environment.

• Working knowledge of GLP, GCLP, or broader GxP regulations.

• Current Hepatitis B vaccination.

Why Apply?

✅ Work on innovative research projects supporting drug discovery and development
✅ Join a collaborative and highly scientific environment
✅ Take ownership of projects and make a direct impact on study outcomes
✅ Develop your career within a growing organisation committed to scientific excellence

Senior Regulatory CMC Consultant – ADC Linker-Payload Drug Substance

6-Month Contract (Renewable) Remote – Europe

Opportunity

An exciting opportunity has arisen for an experienced Senior Regulatory CMC Consultant to support a late-stage oncology programme focused on Antibody Drug Conjugates (ADCs). This is a high-impact consultancy position where you will lead the global regulatory strategy for the linker-payload drug substance component of an innovative ADC programme as it progresses towards major regulatory submissions.

Working within a collaborative Regulatory CMC environment, you will play a critical role in ensuring that the drug substance regulatory package is submission-ready for both European and US health authorities.

This is a fully remote position within Europe offered initially as a 6-month contract with strong likelihood of extension.

Key Responsibilities

Lead Regulatory CMC strategy for the ADC linker-payload drug substance
Provide strategic guidance for global regulatory submissions, including FDA and EMA marketing applications
Drive development and review of Module 3 drug substance documentation
Ensure compliance with current ICH, FDA and EMA regulatory expectations
Support health authority interactions and responses to regulatory questions
Collaborate extensively with CMC, Analytical Development, Process Development, Quality and Manufacturing teams
Contribute to regulatory risk assessments and mitigation strategies
Provide expert advice on drug substance control strategies, specifications, characterisation and stability packages
Support programme teams through critical development and submission milestones

Candidate Profile

Essential Experience

Approximately 10 years or more of Regulatory CMC experience
Strong background in drug substance development
Proven experience leading CMC drug substance aspects of global regulatory submissions
Deep understanding of Module 3 Quality documentation
Excellent working knowledge of ICH, FDA and EMA regulatory requirements
Experience supporting late-stage development or registration programmes

Highly Desirable

Antibody Drug Conjugate (ADC) experience
Linker-payload development experience
Highly potent API (HPAPI) experience
Bioconjugate or complex biologics experience
Experience supporting Marketing Authorisation Applications (MAA), BLAs or equivalent global filings

EU Rate - €500-€600 p/day

Regulatory, CMC, ADC, drug, substance, submission, antibody, conjugate, BLA, MAA, marketing, authorisation, FDA, EMA, module

Senior Clinical Research Associate 
Location: Fully remote with travel across England

 
About Our Client
Our client is a well-established clinical research organisation operating within highly regulated environments, supporting complex, international clinical trials. Working across multiple therapeutic areas and trial phases, they focus on high-quality monitoring, balanced performance expectations and clear career pathways for their clinical operations professionals.
Our client’s team is known for promoting from within, supporting long-term careers in clinical research and offering flexible working arrangements that respect work-life balance. You will be joining a collaborative group of CRAs, study managers and operational specialists who share knowledge and support each other across remote locations.
 
The Opportunity
This is a permanent, fully remote Senior CRA. You will work across a variety of clinical trials and phases without being limited to specific therapeutic areas, giving you broad exposure and the chance to deepen your monitoring expertise.
The role offers a visible pathway for progression, with genuine potential to move quickly through levels based on performance and capability. You will benefit from balanced KPIs, realistic expectations around travel and a supportive structure that focuses on your development rather than simply maximising visit numbers.
 
Key Responsibilities
• Conduct independent on-site monitoring visits across England
• Perform all aspects of routine monitoring activities in line with protocols, SOPs and regulatory requirements across various trial phases.
• Build and maintain strong relationships with site staff to support study conduct, data quality and patient safety.
• Document monitoring activities comprehensively and ensure timely follow-up on action items.
• Collaborate closely with project teams, contributing to study management discussions and resolving site-related issues.
• Demonstrate flexibility around travel and site allocation, understanding that locations may vary according to business needs.
 
What Makes This Role Attractive
• Clear and visible career progression with examples of rapid promotion where merited.
• Balanced KPIs that allow you to focus on quality, development and long-term growth rather than only meeting high visit targets.
• Genuine work-life balance, supported by remote working and thoughtful study allocation.
• An approach to site allocation that aims to maintain reasonable travelling distance, while recognising that some longer trips may be required.
• Access to peer and buddy programmes, offering mentoring, support and guidance from more experienced colleagues.
• Opportunities to progress into other suitable career pathways, depending on your interests and strengths.
 
Skills & Experience Required
• Strong, independent on-site monitoring experience in clinical trials
• Experience across any therapeutic areas and clinical trial phases, studies can be assigned based on individuals experience 
• A valid driving licence and willingness to travel regularly for site visits.
• Life Sciences degree or relevant experience
• Right to work in the UK is essential; our client is unable to offer visa sponsorship.
 

Is This Role Right For You?
This position will suit you if you are an experienced CRA who values structured progression, realistic monitoring expectations and genuine work-life balance. If you enjoy independent on-site work, want to broaden your exposure across different studies and phases, and are looking for a remote role that still offers strong team connection and support, this could be an excellent next step.
 
How to Apply
If you meet the criteria outlined and would like to be considered, please submit your CV. We will review your experience, discuss your career ambitions and guide you through the next steps with our client.

Principal / Lead Clinical Research Associate

Location: UK -Fully remote with travel across England

 
About Our Client
Our client is a well-established clinical research organisation operating within highly regulated environments, supporting complex, international clinical trials. Working across multiple therapeutic areas and trial phases, they focus on high-quality monitoring, balanced performance expectations and clear career pathways for their clinical operations professionals.
Our client’s team is known for promoting from within, supporting long-term careers in clinical research and offering flexible working arrangements that respect work-life balance. You will be joining a collaborative group of CRAs, study managers and operational specialists who share knowledge and support each other across remote locations.
 
The Opportunity
This is a permanent, fully remote Principal CRA role where you will be expected to have established experience in a CRA role, ideally 6 years or more. You will work across a variety of clinical trials and phases without being limited to specific therapeutic areas, giving you broad exposure and the chance to deepen your monitoring expertise.
The role offers a visible pathway for progression, with genuine potential to move quickly through levels based on performance and capability. You will benefit from balanced KPIs, realistic expectations around travel and a supportive structure that focuses on your development rather than simply maximising visit numbers.
 
Key Responsibilities
• Conduct independent on-site monitoring visits across England with over site of a number of locations 
• Perform all aspects of routine monitoring activities in line with protocols, SOPs and regulatory requirements across various trial phases.
• Build and maintain strong relationships with site staff to support study conduct, data quality and patient safety.
• Document monitoring activities comprehensively and ensure timely follow-up on action items.
• Collaborate closely with project teams, contributing to study management discussions and resolving site-related issues.
• Demonstrate flexibility around travel and site allocation, understanding that locations may vary according to business needs.
 
What Makes This Role Attractive
• Clear and visible career progression to further expand your career
• Balanced KPIs that allow you to focus on quality, development and long-term growth rather than only meeting high visit targets.
• Genuine work-life balance, supported by remote working and thoughtful study allocation.
•• Access to peer and buddy programmes, offering mentoring, support and guidance from more experienced colleagues.
• Opportunities to progress into other suitable career pathways, depending on your interests and strengths.
 
Skills & Experience Required
• Strong, independent on-site monitoring experience in clinical trials,
• A proven track record of handling complex studies and responsibilities.
• Experience across any therapeutic areas and clinical trial phases 
• A valid driving licence and willingness to travel regularly for site visits.
• Life Sciences degree or relevant experience
• Right to work in the UK is essential; our client is unable to offer visa sponsorship.
 
Is This Role Right For You?
This position will suit you if you are an experienced CRA who values structured progression, realistic monitoring expectations and genuine work-life balance. If you enjoy independent on-site work, want to broaden your exposure across different studies and phases, and are looking for a remote role that still offers strong team connection and support, this could be an excellent next step.
 
How to Apply
If you meet the criteria outlined and would like to be considered for Principal CRA level position, please submit your CV. We will review your experience, discuss your career ambitions and guide you through the next steps with our client.