- Company: Celerion
- Location: UK
- Salary: Pay not listed
- Work type: Remote
Celerion at a glance
celerion.com- Founded 2010
SEC filings mentioning "Celerion": 187 — search EDGAR
1,288 employees covered under a retirement plan (2023 filing) — via DOL Form 5500 / EFAST2
Registered as a global legal entity (LEI 549300LVRF1S56CIE823, US) — via GLEIF
Celerion is a pharmaceutical services company (founded 2010) focused on clinical research and bioanalytical work. Recent coverage includes ownership change activity: H.I.G. Capital’s sale of the firm, THL’s reported ~$1.8B acquisition plans, and expansion of its Zurich bioanalytical laboratory to meet demand (PR Newswire, Axios, Business Wire).
Trial Master File Representative - Celerion - Remote (UK)
About This Position
Celerion, a leading drug research company, is seeking a Trial Master File Representative to join our dynamic team. This role will be based remotely within the UK and involves preparing and maintaining comprehensive Trial Master Files for both internal and external studies.
Core Duties
- Create and maintain structured Trial Master Files that comply with protocol and regulatory requirements.
- Communicate effectively with client sponsors, project managers, monitors, sites, and other study contacts to ensure compliance.
- Ensure the completeness and accuracy of all trial documentation within the TMF.
What We're Looking For
- Full and permanent right to work in the UK.
- Experience in clinical research or a related field is preferred.
- Strong organizational skills with attention to detail.
- Excellent communication and interpersonal skills.
- Familiarity with regulatory requirements for clinical trials.
About the Company
Celerion is a performance-driven drug research company operating in robust and growing markets. We offer a competitive salary in a strong developmental environment where every employee contributes to making a distinctive impact on global health and well-being. Our team thrives on a sense of purpose, working together to drive innovation and excellence.
Applying for This Role
Celerion is an equal opportunity employer committed to diversity and inclusion. To apply, complete your application directly on this page, or you'll be redirected to the employer's application platform to finish submitting there.
You’ll finish your application on the employer’s website. We don’t ask for a resume on this page.
Explore Celerion online
What people say about Celerion
Recent news
- H.I.G. Capital Completes Sale of Celerion, Highlighting a Period of Robust Exit Activity - PR Newswire
- M c Dermott Will & Schulte advises H.I.G. Capital in the sale of Celerion - McDermott Will & Schulte
- THL plans $1.8B deal for pharma services firm Celerion - Axios
- Celerion Expands Zurich Bioanalytical Laboratory to Meet Growing Market Demand - Business Wire
- Celerion expands Swiss bioanalytical laboratory capacity - Pharmafile
Latest from Celerion
- Celerion Expands Zurich Bioanalytical Laboratory to Meet Growing Market Demand
- Cocktail DDI Studies: Myths vs. Facts
- The Resurgence of Antibody Drug Conjugates: How ADCs are taking over oncology (again) and what we’ve learned about creating bioanalytical methods to support preclinical and clinical success.
Aggregated from public discussions and news; opinions are the authors’ own.
Working in UK
This role is remote in the United Kingdom. The UK (England, Scotland, Wales, and Northern Ireland) is a northwestern European country of roughly 69 million people, so remote TMF work typically means UK hours, data-protection norms, and clinical-document standards rather than a fixed site commute.
🇬🇧 Relocation safety for United Kingdom: Exercise Normal Caution — via Warnely, CC BY 4.0
National unemployment rate in United Kingdom: 4.7% — via World Bank
GDP per capita in United Kingdom: $57,602 — via World Bank
Consumer price inflation in United Kingdom: 3.9% (annual) — via World Bank
Real GDP growth in United Kingdom: 1.4% (annual) — via World Bank
Average hours worked per year in United Kingdom: 1,533 — via OECD
Build the skills for this role
Build strength in eTMF platforms, ICH GCP document expectations, TMF Reference Model structure, and precise QC of essential documents. Practice clear written follow-up with CRAs, study managers, and vendors; no paid certification list was supplied for this posting.
- Walk through how you QC and file a late or incomplete essential document without losing chain of custody.
- Explain inspection readiness: what you check before a monitor or auditor reviews the TMF.
- Describe remote collaboration when study teams miss document deadlines.
Strong fit if you like detail-heavy document control in clinical research, can work independently remotely in the UK, and care about audit-ready TMF quality more than patient-facing or lab work.
Job details above are provided by the employer/source. The sections on this page are compiled from public data sources with AI assistance.
Accommodations: if you need a workplace accommodation to apply for or perform this job, see ADA.gov or EEOC.gov for guidance on your rights and how to request one.
Listing facts
- Role Trial Master File Representative (Remote)
- Employer Celerion
- Location UK · Remote-friendly
- Type Full Time
- Pay (from listing) Pay not listed
- Posted August 12, 2026
- Apply by September 11, 2026
- Country United Kingdom
- Overview Full job description on this page (232 words)
Facts above come from this job record on Get A Job.AI — not copied from third-party review sites.
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Attributed public threads and profiles — not employee reviews or star ratings.
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