Clinical Research Associate II – Spanish, Portuguese, English

🔥 1 hour ago

🇵🇹 Portugal – Remote

⏰ Full Time

🟠 Senior

🧪 Clinical Research

👻 Ghost score 18%

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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ERGOMED

WebsiteLinkedInAll Job Openings

1001 - 5000 employees

Founded 1997

💼 Consulting

🏥 Healthcare

📦 Logistics

Consulting • Healthcare • Logistics

ERGOMED is a global group providing specialized services to the biotechnology and pharmaceutical industries. It operates under different service lines, including Ergomed Clinical Research, PrimeVigilance, and ADAMAS Consulting, and is dedicated to providing full-service clinical research organization (CRO) capabilities. Focused on oncology, rare diseases, and complex trials, it also offers end-to-end pharmacovigilance and medical information services, as well as comprehensive GxP audits. Ergomed is committed to supporting drug development with a global presence in around 100 countries.

📋 Description

• Perform on-site or remote Pre-Study, Initiation, Interim, and Close-Out monitoring visit activities in Spain and Portugal • Ensure facilities and investigational-site staff remain adequate throughout the study • Identify investigators and verify their qualifications, resources, facilities, equipment, and staff • Train investigational-site staff as necessary • Support preparation of regulatory and/or EC submissions when applicable • Help bring safe and effective pharmaceutical treatments to patients through clinical research

🎯 Requirements

• College/University degree in Life Sciences or an equivalent combination of education, training & experience • Extensive on-site monitoring experience in phase 2/3 trials • Ideally, experience with complex trials such as oncology / rare disease • Full working proficiency in English, Spanish & Portuguese • Ability to plan, multitask and work in a dynamic team environment • Communication, collaboration, and problem-solving skills • Ability to travel

🏖️ Benefits

• Work remotely • Work-life balance • Collaborative, international team environment • Career growth opportunities • Trusted to take ownership early • Passionate and collaborative team of clinical research, pharmacovigilance, and quality consulting experts