Regional Clinical Compliance Manager

🕒 July 10

🇳🇱 Netherlands – Remote

💵 €88.8k - €111k / year

⏰ Full Time

🟠 Senior

🔴 Lead

🚔 Compliance

👻 Ghost score 15%

What it means: how likely this posting is sitting open without active hiring.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.How we score it: age, reposts, open roles vs team size, how fast jobs close, and whether pay is listed.Fine print: an estimate from public data, not a judgment of the company. Real jobs can score high, so treat it as a hint, not a fact.

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BeOne Medicines

WebsiteLinkedInAll Job Openings

10,000+ employees

Founded 2010

🧬 Biotechnology

🏥 Healthcare

💊 Pharmaceuticals

Biotechnology • Healthcare • Pharmaceuticals

BeOne Medicines is a global oncology company domiciled in Switzerland that is discovering and developing innovative treatments that are more affordable and accessible to cancer patients worldwide. With a portfolio spanning hematology and solid tumors, BeOne is expediting the development of its diverse pipeline of novel therapeutics through its internal capabilities and collaborations. With a growing global team of more than 11,000 colleagues spanning six continents, the Company is committed to radically improving access to medicines for far more patients who need them.

📋 Description

• Serve as the primary compliance subject matter expert for country teams regarding GCP requirements, company and study-specific procedures, and compliance-related queries. • Provide expert guidance and interpretation of regulations and internal standards. • Analyze and confirm initial country and site-specific risks, including critical data and key processes. • Communicate country and site trends and lessons learned to Clinical Operations functions. • Align with Global Clinical Compliance on execution of the Study Health Check Plan at country and site level. • Lead and support key process reviews through remote desk checks. • Identify high-risk sites using a structured, risk-based approach. • Conduct Site Compliance Visits at identified high-risk sites. • Support country teams in identifying, managing, and resolving compliance issues. • Support and manage Corrective and Preventive Actions (CAPAs), including risk assessment, root cause analysis, effectiveness measures, and timely action completion. • Support the Regional Clinical Compliance Inspection and Audit Support team with site audits and inspections. • Safeguard patient safety, data integrity, and inspection readiness.

🎯 Requirements

• Bachelor’s degree (BS/BA or equivalent) or higher in a scientific, medical or healthcare discipline with a minimum of 5 years of progressive experience in clinical operations roles plus minimum 4 years’ experience in a GCP compliance or equivalent role (i.e. quality) is preferred. • Experience in oncology global trials is preferred. • Exceptions may be made for candidates with equivalent appropriate Clinical Operations experience. • Understanding of clinical trial processes with a thorough knowledge of ICH-GCP and associated regulatory guidelines • Analytical and problem-solving skills • High attention to detail and quality orientation • Excellent English written and verbal communication and interpersonal skills • Excellent organizational skills and ability to prioritize and multitask • Ability to work independently in a multi-cultural setting and effectively handle multiple priorities in a fast-paced environment • PC literacy required; MSOffice skills (Outlook, Word, Excel, PowerPoint)

🏖️ Benefits

• Equal opportunity employment • Travel up to 20% or less