Clinical Research Associate I

🔥 0 minutes ago

🇪🇸 Spain – Remote

⏰ Full Time

🟢 Junior

🟡 Mid-level

🧪 Clinical Research

🚫👨‍🎓 No degree required

👻 Ghost score 10%

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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AbbVie

WebsiteLinkedInAll Job Openings

10,000+ employees

Founded 2013

🏥 Healthcare

💼 Consulting

🏭 Manufacturing

Healthcare • Consulting • Manufacturing

AbbVie is a global pharmaceutical company that discovers and delivers innovative medicines and solutions to enhance lives. With a focus on addressing the world's toughest health challenges, AbbVie operates in over 175 countries, providing a wide range of products across areas like immunology, oncology, neuroscience, and aesthetics. Committed to scientific innovation, AbbVie invests heavily in research and development, aiming to produce first-in-class medicines. The company also emphasizes workplace diversity, sustainability, and patient support initiatives, ensuring positive impact for both its patients and the broader community.

📋 Description

• Monitor activities conducted by clinical investigative sites for AbbVie clinical studies • Ensure protocol execution, regulatory compliance, GCP/ICH Guidelines, AbbVie SOPs, monitoring plans, and quality standards • Conduct site qualification, initiation, interim monitoring, and study closeout visits for Phase 1–4 studies • Oversee site personnel activities and motivate or influence them to meet study objectives • Proactively manage sites and implement action plans to ensure compliance and inspection readiness • Ensure quality and timely submission of study-site data, including safety-event reporting and follow-up • Ensure study-subject safety and protection through monitoring-plan, SOP, guideline, and regulatory compliance • Train study-site personnel on protocols and regulatory requirements • Manage investigator payments and negotiate investigator/hospital agreements • Complete expense reports according to applicable guidelines • Identify, evaluate, and recommend potential investigators and clinical sites

🎯 Requirements

• Appropriate tertiary qualification in a health-related field (e.g., Medical, Scientific, Nursing) preferred • Clinical Trials Master’s Degree preferred • Minimum of 1 year of clinically related experience • Preferably 6 months of independent clinical research monitoring or Study Coordinator experience • Experience in on-site monitoring of investigational drug or device trials required • In-depth knowledge of therapeutic indications relevant to clinical trials • In-depth knowledge of clinical research regulations, ICH/GCP Guidelines, and applicable regulations • Strong planning and organizational skills • Ability to work effectively and efficiently in a dynamic environment with competing projects and deadlines • Ability to understand and follow work processes within the assigned function • Strong analytical and conceptual capabilities • Interpersonal skills and ability to communicate clearly • Ability to address clinical site issues with appropriate guidance and initiate and communicate corrective action • Ability to use functional expertise and exercise good judgment

🏖️ Benefits

• Employees can work remotely • Equal opportunity employer • Commitment to operating with integrity, driving innovation, transforming lives and serving the community