Associate Consultant RA & Publishing

TRIUM Clinical Consulting NV; Oxford; Hybrid; GBP 26,000 - 38,000; Full time

Job summary

TRIUM Clinical Consulting NV seeks an Associate Consultant to join the Regulatory Affairs & Publishing team on a hybrid basis in the UK. The role targets early-career professionals eager to develop in regulatory submissions and dossier publishing for pharma, biotech and medical devices.

You will start with day-to-day activities, gradually taking on more responsibility, while benefiting from mentoring and a collaborative team across life sciences.

Qualifications

• University degree in a scientific discipline.
• No prior Regulatory Affairs experience required, internships welcome.
• Knowledge of CTD/eCTD or EU regulatory procedures is advantageous but not required.
• Interest in Regulatory Affairs and regulatory submissions.
• Willingness to learn and attention to detail.

Responsibilities

• Support preparation and organisation of regulatory submission documents.
• Assist with formatting, quality checking of regulatory documents.
• Support preparation and maintenance of eCTD dossiers under supervision.
• Assist with regulatory submissions and related administrative tasks.
• Maintain submission trackers and project documentation.

Skills

Attention to detail

Organisational skills

Analytical thinking

Communication skills

English proficiency

Problem solving

Education

University degree in Pharmacy/Life Sciences/Chemistry/Biotechnology/Biomedical Sciences

Tools

Microsoft Office

Job description

Associate Consultant RA & Publishing

Location: QbD UK - hybrid
Type: Full-time

We are looking for a motivated and curious Associate Consultant to join our Regulatory Affairs & Publishing team.

This is an exciting opportunity for someone at the beginning of their career who is interested in the pharmaceutical and life sciences industry and wants to develop their knowledge of Regulatory Affairs, regulatory submissions and dossier publishing.

We are looking for someone with a strong scientific foundation, attention to detail, a willingness to learn, and an interest in developing a career in regulatory consulting.

You will work closely with experienced colleagues and gradually take on more responsibility as your knowledge and confidence grow.

What’s in it for you?

Make a real impact: Contribute to shaping the future of the Life Sciences industry by supporting innovative projects and clients across pharma, biotech and medical devices

Grow within a community of experts:Benefit from knowledge-sharing, mentoring, and exposure to diverse, challenging assignments that broaden your expertise.

Build a meaningful career:As an ambitious and pioneering company, we want to offer you the best possible environment to thrive within the life sciences.

A fair, competitive package: We offer tailored, transparent compensation aligned with your expertise, preferences, and local market regulations — because your contribution deserves to be valued.

What you’ll be doing

As an Associate Consultant, you will support the Regulatory Affairs & Publishing team with day-to-day activities and gradually develop your ability to manage tasks independently.

Your responsibilities may include:

• Supporting the preparation and organisation of regulatory submission documents.
• Assisting with the compilation, formatting, and quality checking of regulatory documentation.
• Supporting the preparation and maintenance of eCTD dossiers under the guidance of experienced colleagues.
• Assisting with regulatory submissions and related administrative activities.
• Helping to maintain submission trackers, project documentation, and regulatory records.
• Supporting the preparation and review of documents such as Module 1 content and product information.
• Performing document checks to ensure that information is complete, accurate, and consistent.
• Supporting the team with publishing activities and electronic submission processes.
• Conducting basic research into regulatory requirements and guidelines.
• Helping to monitor regulatory changes and sharing relevant information with the team.
• Supporting client projects and internal Regulatory Affairs activities.
• Working collaboratively with colleagues across Regulatory Affairs and other life sciences functions.

As you gain experience, you will have the opportunity to take ownership of more complex tasks and contribute more independently to client projects.

What you bring

• A university degree in Pharmacy, Life Sciences, Chemistry, Biotechnology, Biomedical Sciences, or a related scientific discipline.
• No previous Regulatory Affairs experience is required. Relevant internships, university projects, placements, or experience in the pharmaceutical/life sciences industry are welcome but not essential.
• Knowledge of CTD/eCTD, EU pharmaceutical legislation, regulatory procedures, or electronic submission systems would be an advantage, but is not required.
• An interest in pharmaceutical Regulatory Affairs and regulatory submissions.
• A willingness and ability to learn new concepts, regulations, and processes.
• Good attention to detail and a careful approach to working with documents and data.
• Good organisational skills and the ability to manage several tasks with appropriate guidance.
• Basic analytical and problem-solving skills.
• Good written and verbal communication skills.
• Good knowledge of English, both written and spoken.
• Good working knowledge of Microsoft Office, particularly Word and Excel.
• A proactive attitude and willingness to ask questions when something is unclear.

Who you are

Our culture is driven by values If this sounds like you, you’ll fit right in:

• You’re resilient and tackle challenges with a positive mindset
• You’re curious and always up for learning something new
• You have a no non-sense approach honest, clear, respectful
• You’re innovative and bring ideas, not just opinions
• And above all, you’re serious about your work, but not too serious about yourself

About us

We support life sciences companies from idea to patient — offering tailored solutions in development, clinical, regulatory, compliance, production, and distribution. With 500+ experts across 8 countries, we help drive innovation in ATMP, biotech, medical devices, diagnostics, digital health, and pharma.

We believe in JPEG:
Joy. Partnership. Going the Extra Mile. Getting Things Done.

You won’t just be taking a job — you’ll be joining a community where people grow, laugh, build, and contribute to something bigger.