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- Tasks: Gain hands-on lab experience and support key research activities in a regulated environment.
- Company: Belfast-based Clinical Research Organisation focused on precision medicine.
- Benefits: Mentorship, exposure to cutting-edge technology, and meaningful research contributions.
- Why this job: Make a real impact on patient care while learning from industry experts.
- Qualifications: Pursuing a degree in Biomedical Science or related field with basic lab skills.
- Other info: Join a dynamic team and enhance your career in clinical research.
The predicted salary is between 13 - 16 ÂŁ per hour.
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.
Role Overview
This placement provides an exciting opportunity for a motivated student to gain hands‑on laboratory experience in a high‑quality, regulated laboratory environment. The successful candidate will support key research and development activities, including assay validation, pre‑clinical assay revalidation, and routine laboratory management tasks. This role will allow the student to work closely with experienced scientists and contribute to real‑world applications of diagnostic technology.
Key Responsibilities
- Assist in the development, validation, and revalidation of diagnostic assays (IHC, PCR, ELISA).
- Support the transfer of pre‑clinical biomarker assays to ARC Research Laboratories, ensuring compliance with US FDA IDE and EU IVDR regulations.
- Participate in transitioning research‑use‑only (RUO) assays to investigational‑use‑only (IUO) and IVDR‑compliant formats.
- Contribute to the routine maintenance and installation of laboratory equipment.
- Follow Good Clinical Practice (GCP) guidelines and ensure compliance with relevant quality and regulatory standards (CAP CLIA, and ISO 17025).
- Support routine laboratory tasks, including sample preparation, data recording, stock and order management.
- Work collaboratively with research scientists, regulatory teams, and clinical trial partners to help ensure project objectives are met.
Key Skills & Competencies
- Currently pursuing a degree in Biomedical Science, Molecular Biology, Biochemistry, or a related field.
- Strong basic laboratory skills, with interest in developing experience in molecular and immunological techniques (PCR, ELISA, IHC).
- Ability to work independently and within a team in a fast‑paced research environment.
- Excellent attention to detail and strong analytical skills.
- Effective communication and organisational skills.
What We Offer
- Hands‑on experience in a cutting‑edge diagnostic research laboratory.
- Exposure to regulatory and quality assurance processes in a highly regulated industry.
- Mentorship from experienced professionals in diagnostic technology and clinical research.
- An opportunity to contribute to meaningful research that impacts patient care and clinical trials.
We are an equal opportunity employer; applications are welcome from all and appointment will be made on the basis of merit.
Benefits
- Parking
Laboratory Placement Student in Belfast employer: ARC Regulatory
Contact Detail:
ARC Regulatory Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Laboratory Placement Student in Belfast
✨Tip Number 1
Network like a pro! Reach out to professionals in the field through LinkedIn or industry events. A friendly chat can open doors that a CV just can't.
✨Tip Number 2
Prepare for interviews by researching ARC and its projects. Show us you’re genuinely interested in our work with precision medicine and how you can contribute.
✨Tip Number 3
Practice your lab skills! Brush up on techniques like PCR and ELISA, so you can confidently discuss them during interviews. We love seeing candidates who are hands-on.
✨Tip Number 4
Apply through our website! It’s the best way to ensure your application gets noticed. Plus, it shows us you’re keen on being part of our team at ARC.
We think you need these skills to ace Laboratory Placement Student in Belfast
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the Laboratory Placement Student role. Highlight any relevant coursework, lab skills, and experiences that align with the job description. We want to see how your background fits with our mission at ARC!
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to express your passion for biomedical science and how you can contribute to our team. Be sure to mention specific projects or experiences that relate to the responsibilities outlined in the job description.
Showcase Your Skills: In your application, don’t just list your skills—show us how you've used them! Whether it's PCR, ELISA, or IHC techniques, provide examples of how you've applied these in your studies or previous roles. We love seeing practical experience!
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 ARC!
How to prepare for a job interview at ARC Regulatory
✨Know Your Science
Brush up on your knowledge of molecular biology, biochemistry, and the specific techniques mentioned in the job description, like PCR and ELISA. Being able to discuss these topics confidently will show that you're not just interested but also knowledgeable about the field.
✨Understand Regulatory Standards
Familiarise yourself with Good Clinical Practice (GCP) guidelines and relevant regulations like CAP CLIA and ISO 17025. This will demonstrate your commitment to compliance and quality assurance, which are crucial in a clinical research environment.
✨Show Your Team Spirit
Prepare examples of how you've worked effectively in teams or independently in fast-paced environments. Highlighting your ability to collaborate with scientists and regulatory teams will resonate well with the interviewers.
✨Ask Insightful Questions
Prepare thoughtful questions about ARC's projects, the ARC360 platform, or the specific assays you'll be working on. This shows your genuine interest in the role and helps you understand how you can contribute to their mission.
