Senior Clinical Research Associate

🕒 July 21

🇳🇱 Netherlands – Remote

⏰ Full Time

🟠 Senior

🧪 Clinical Research

👻 Ghost score 55%

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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WEP Clinical

WebsiteLinkedInAll Job Openings

51 - 200 employees

Founded 2008

💼 Consulting

📦 Logistics

💊 Pharmaceuticals

Consulting • Logistics • Pharmaceuticals

WEP Clinical is a Pharmaceutical Services Provider that specializes in Drug Development Programs, Treatment Access Solutions, and Market Access and Commercialization. The company focuses on providing critical support throughout the entire drug development and commercialization journey, helping sponsors advance their medicines and improve patient access. WEP Clinical offers services such as clinical trial services, expanded access programs, post-approval named patient programs, and market access consulting, ensuring that much-needed therapies reach patients worldwide.

📋 Description

• Oversee all aspects of clinical monitoring and site management in compliance with GCP, global regulatory requirements, and WEP Clinical SOPs • Conduct on-site and remote monitoring to ensure protocol adherence • Maintain essential documentation and inspection-ready site and patient data • Build relationships with sponsors and sites as a key study contact • Support development of study-specific procedures, including Monitoring Plans • Assist with training or coordinating other CRAs • Contribute to study document design and review, including protocols, CRFs, ICFs, and study plans • Lead site feasibility activities, including questionnaires, SQVs, and site recommendations • Plan and conduct SIVs, routine monitoring, and close-out visits • Train site staff on protocol compliance and regulations • Verify source data and CRFs for completeness, accuracy, and consistency • Review IP accountability, safety event documentation, and protocol deviations • Drive corrective and preventative actions • Manage and resolve data queries and analyze error trends • Track and close action items and maintain oversight of monitoring deliverables • Support investigator meetings and internal/external meetings • Contribute to SOPs, monitoring tools, and templates • When assigned as Lead CRA, oversee complex studies, develop monitoring documents, finalize visit reports, train/coordinate CRAs, and handle CRA escalations

🎯 Requirements

• Bachelor’s degree (life sciences, nursing, or related field preferred) • 5–7+ years’ experience conducting on-site and remote monitoring visits (or equivalent clinical research experience) • Senior CRA levelling: SCRA I (3–5 yrs); SCRA II (5+ yrs) • Broad therapeutic exposure across multiple study types and indications • Strong technical/scientific aptitude and ability to execute clinical protocols • Advanced organizational and logistical skills; ability to manage multiple sites/protocols within budget and timelines • Excellent written and verbal communication and stakeholder engagement • Understanding of medical/therapeutic areas and medical terminology • Ability to train, coach, and mentor clinical research staff • Proficiency with MS Office and EDC systems • Willingness to travel up to 80% • Resume must be submitted in English

🏖️ Benefits

• Wellness, growth, development, and team relationship initiatives • Inclusive, supportive work environment • Team events • Smoke-free, drug-free, and alcohol-free work environment • Reasonable accommodation for qualified individuals with known disabilities