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For Companies At a Glance
- Tasks: Join our lab team to design and execute cutting-edge clinical studies.
- Company: Belfast-based Clinical Research Organisation focused on precision medicine.
- Benefits: Competitive salary, professional development, and a dynamic work environment.
- Why this job: Make a real impact in healthcare by advancing precision medicine for patients globally.
- Qualifications: Bachelor's degree in biological sciences and 3+ years of relevant lab experience.
- Other info: Work in a fast-paced, innovative setting with excellent career growth opportunities.
The predicted salary is between 36000 - 60000 £ per year.
ARC\’s purpose is to expedite access to precision medicine clinical trials for patients globally. We fulfil our purpose through our dedicated team of experts with unparalleled domain knowledge, and the important relationships we have developed with our global clients.
We are a Belfast-based Clinical Research Organisation that specialises in delivering compliance excellence for companies in the precision medicine sector. We support many of the world\’s leading pharmaceutical R&D companies in implementing unapproved diagnostics in their clinical development programmes for patient selection or stratification, working as a strategic and integrated expert partner, taking full sponsor ownership of the IVD study being conducted in parallel with our clients\’ IND/IMP trial.
ARC\’s team of experts cover IVD regulatory compliance, study design and approvals, quality assurance including vendor due diligence and management along with a team of clinical research experts who manage the IVD study, ensuring it is conducted in compliance with local and global GCP, and that the biomarker data is robust and reliable.
To further support our growing client base and to expedite patient access to life-saving experimental medicines, ARC has developed and launched our SaaS platform, ARC360. ARC360 is transforming how organisations access regulatory intelligence and tailor study-specific information for using in vitro diagnostics to select and manage patients in IND trials. Powered by cutting-edge technologies and supported by a team of regulatory, quality, and clinical operations experts, ARC360 is designed to accelerate the initiation of complex clinical trials.
Job Purpose
To be an integral member and significant contributor to ARCs laboratory team in the design, implementation and execution of internal and client laboratory IVD or CDX studies, ensuring that client objectives are met and exceeded at all times. This will require the utilization of regulated experimental approaches to clinical studies, internal and external stakeholder satisfaction as well as an innate work ethic that aligns with the company’s core values.
Key Responsibilities
- Develop, optimise and validate assay protocols for molecular assays including PCR and Next generation Sequencing
- Conduct experiments to troubleshoot and refine processes to improve assay sensitivity, specificity, and reproducibility.
- Conduct analysis of biomarker levels in biological samples.
- Analyse and interpret experimental data, preparing comprehensive reports and presentations for stakeholders.
- Stay updated with the latest advancements in relevant scientific techniques to inform laboratory activities.
- Maintain accurate laboratory records and ensure compliance with safety and quality standards
Essential Skills & Experience
- Bachelors degree in biological sciences or other related scientific subjects
- Minimum 3+ years’ experience in designing and implementing, PCR/NGS and or ELISA experiments
- Strong understanding of assay verification and validation in line with regulatory standards such as IVDR and CLSI
- Experience working within a regulated laboratory environment (ISO17025/ ISO15189 / CAPCLIA)
- Excellent interpersonal skills and presentation skills
- Excellent problem‑solving skills and the ability to work independently as well as part of a team
- Able to work flexibly as required to ensure business needs are met.
- Proof of Right‑to‑Work in the UK.
- Must be able to commute daily to Belfast as job is 100% on‑site.
Desirable Skills & Experience
- MSC/PhD in biological sciences or other related scientific subjects
- Previous experience in a commercial laboratory
- Experience in IHC/histology
- Prior experience working in a rapid growth, SME environment
- Experience with IVDR/IDE regulation
- HEP B Vaccinated (willingness to be vaccinated at start of role)
Equal Opportunity
We are an equal opportunity employer; applications are welcome from all and appointment will be made on the basis of merit.
Skills: research development Scientist
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Research and Development Scientist employer: ARC Regulatory Ltd
Contact Detail:
ARC Regulatory Ltd Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Research and Development Scientist
✨Tip Number 1
Network like a pro! Reach out to professionals in the precision medicine field on LinkedIn or at industry events. We can’t stress enough how valuable personal connections can be in landing that dream job.
✨Tip Number 2
Prepare for interviews by practising common questions related to R&D and your specific skills. We recommend doing mock interviews with friends or mentors to boost your confidence and refine your answers.
✨Tip Number 3
Showcase your passion for the field! During interviews, share your insights on recent advancements in molecular assays or clinical trials. We want to see your enthusiasm and knowledge shine through!
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, we love seeing candidates who are proactive about their job search.
We think you need these skills to ace Research and Development Scientist
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the Research and Development Scientist role. Highlight your experience with PCR, NGS, and any relevant regulatory standards. We want to see how your skills align with our needs!
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you're passionate about precision medicine and how you can contribute to our team. Keep it engaging and personal – we love to see your personality!
Showcase Your Achievements: When detailing your experience, focus on specific achievements rather than just duties. Did you improve assay sensitivity or streamline a process? We want to know how you made an impact in your previous roles!
Apply Through Our Website: We encourage you to apply directly through our website. It’s the best way for us to receive your application and ensures you’re considered for the role. Plus, it shows you’re keen to join our team at ARC!
How to prepare for a job interview at ARC Regulatory Ltd
✨Know Your Science
Make sure you brush up on your knowledge of molecular assays, PCR, and NGS. Be ready to discuss your experience in designing and implementing these experiments, as well as any challenges you've faced and how you overcame them.
✨Showcase Your Problem-Solving Skills
Prepare examples of how you've tackled complex issues in the lab. Think about specific instances where you improved assay sensitivity or dealt with unexpected results. This will demonstrate your analytical thinking and adaptability.
✨Understand Regulatory Standards
Familiarise yourself with IVDR and CLSI regulations, as well as ISO standards like ISO17025 and ISO15189. Being able to speak confidently about compliance and quality assurance will show that you’re a good fit for their regulated environment.
✨Engage with Stakeholders
Since you'll be preparing reports and presentations, practice how you communicate complex data to different audiences. Highlight your interpersonal skills and how you’ve successfully collaborated with team members and clients in the past.
